22 Research jobs in County Dublin
Research Analyst
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About us
From day one, you'll notice there is something special about working at Davy. Our success is built on nearly 100 years of forging strong relationships with our clients and developing the careers of Ireland's future business leaders.
Established in 1926, the Davy Group sits at the heart of wealth and capital in Ireland, providing a broad range of services to high-net-worth individuals, self-directed investors, small-to-medium enterprises, credit unions, corporations, and domestic & international institutional investors.
Our culture is shaped around three values, which are at the heart of everything we do: client success, one Davy, and building a proud legacy. Sharing the same goals, we work together to deliver exceptional outcomes for our clients. As part of a team of over 900, you will be encouraged to learn and to grow, both professionally and personally.
About the role
An opportunity has arisen for a Research Analyst to join the Industrials team within the Research department at Davy. The purpose of the position is to assume responsibility for coverage of the Irish and International Industrial sector with specific responsibility for coverage of certain listed stocks within the sector. In the role, the successful candidate will:
- Formulation and regular review of stock views based on detailed industry, company and financial analysis.
- Work as an integral part of the team covering all aspects of the Industrials sector including monitoring market developments, interpreting data and market trends.
- Regular written, including in-depth company and thematic research on the stocks/sector under coverage.
- Regular communication (including presentations) with clients (internal and external) with sector updates, relevant news, information and potential trading opportunities.
- Extensive financial modelling and sensitivity analysis.
- Utilisation of various stock market and corporate valuation techniques.
- Comply with the Risk and Compliance frameworks, policies and procedures associated with the role.
We are looking for somebody who has the following background and skills:
- Excellent analytical and modelling skills including creating and interpreting models.
- Excellent communication and presentation skills, both verbal and written.
- c. 3 years' experience in Accounting, Equity Research, Investment Banking or the Industry.
- An Accounting qualification preferable, CFA, MBA also recognised.
- Experience writing in a professional capacity, e.g. crafting equity research notes / correspondence; presentation and/or development of industry reports.
- Natural curiosity, critical thinking and logical evaluation.
- Ability to work independently and part of a team.
- Strong interpersonal skills.
What we offer
We offer a range of benefits and experiences to support your professional and personal growth, whatever your career stage. Our benefits are not just a number. Yes, we offer competitive salary, annual performance-related discretionary bonus, annual flexible benefits, employer pension contribution, and multiple insurance coverage. But more than that, we focus on developing our people to be their best, professionally and personally.
Training support provided by award-winning Learning & Development Team, extensive sports & social programmes (including free on-site gym & fitness studio), flexible working options, employee assistance programme, enhanced leave options, and social & community care initiatives are just some of the ways our people can empower themselves to be their best.
Important Information
The position set out above is defined in the Fitness & Probity Standards issued by the Central Bank of Ireland ("Fitness & Probity Standards") as a "Controlled Function (CF)", namely CF4. Therefore there is a requirement to hold, or be willing to take one of the following exams: APA (Regulation & Investment) or Registered Stockbroker or QFA. In compliance with the Fitness and Probity Standards applicable to your position, any offer of employment is conditional upon you demonstrating that you meet the Fitness & Probity Standards.
Davy is an equal opportunities employer, committed to fostering an inclusive and diverse workplace. We value diversity in both background and experience, and even if you don't meet all of the requirements outlined in the job description, we still encourage you to apply. We review all applications received. As part of our commitment to creating an accessible environment, we want to ensure that everyone has an equal opportunity to participate in the interview process. If you require any reasonable accommodations, please let us know, and we will do our best to make the necessary arrangements.
Appointment to this role is subject to the candidate's eligibility to work in Ireland.
Where agency assistance is required, our Recruitment Team will engage directly with suppliers. Unsolicited CVs / profiles supplied to us by recruitment agencies will not be accepted for this role.
Davy Group is a member of the Bank of Ireland Group.
Research Analyst
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Location: UK & Ireland Employment Type: Full-time Reporting to: Director, Destination Strategy
Who We AreTOPOSOPHY is a destination development, marketing, and placemaking agency working at the crossroads of research, strategy, and experience design. For more than 15 years we've supported governments, DMOs, cultural institutions, and global organisations such as the European Travel Commission, Mastercard, UNDP, and UNWTO.
Our work spans the UK, Ireland, and Europe — from national tourism strategies and destination experience development plans to city masterplans and large-scale cultural events.
The RoleWe are looking for a Research Analyst to join our Destination Strategy & Research team. This is a hybrid role, combining analytical rigour with client-facing delivery.
You will contribute to the design and execution of Destination Experience Development Plans (DEDPs), Destination Management Plans (DMPs), and other strategy projects across the UK, Ireland, and Europe. Your work will range from advanced research and data analysis to running stakeholder workshops, public consultations, and presenting findings at industry events.
The right candidate will have experience moving seamlessly between research, strategy, and communication — someone who can both unpack complex data and stand in front of a room of stakeholders to bring it to life.
Key Responsibilities- Research tourism trends, visitor behaviour, and policy developments in the UK, Ireland, and Europe.
- Benchmark DMOs, tourism boards, and destination marketing strategies internationally.
- Design and deliver quantitative and qualitative research, including surveys, interviews, and focus groups.
- Lead or support stakeholder and public consultation processes, from setup to facilitation and reporting.
- Contribute to Destination Experience Development Plans (DEDPs) and Destination Management Plans (DMPs) with insights and evidence.
- Present research and recommendations in client workshops, industry keynotes, and stakeholder meetings.
- Turn complex research outputs into engaging reports, presentations, and communication materials.
- Contribute to the production of white papers, trend reports, and thought-leadership outputs.
- Track emerging trends (sustainability, community-led tourism, digital tools, AI) and bring fresh approaches into projects.
Key Skills & Qualifications
Tourism & Destination Expertise: Deep understanding of tourism trends, destination management, and place branding.
Research & Data Analysis: Strong skills in tourism market analysis, visitor insights, and economic impact research.
- Data Visualization: Experience using GIS, Tableau, or other tools to present research findings effectively.
- Analytical Thinking: Ability to interpret complex tourism data and provide clear strategic recommendations.
- Communication & Writing: Proven ability to write compelling reports, policy briefs, and industry insights.
- Collaboration: Experience working with DMOs, government agencies, tourism boards, and private-sector stakeholders.
- Master's degree in tourism, urban planning, geography, marketing, economics, or a related field.
- 5+ years of research experience in tourism, travel insights, destination strategies, or economic development.
- Strong proficiency in Excel, data visualization tools, and tourism analytics.
- Experience working with destination management organizations, tourism boards, or city marketing agencies.
- Fluent in English (additional languages are a plus).
- Competitive salary and private health insurance
- Work on global projects that impact destinations worldwide
- Career growth and mentorship in a dynamic, collaborative environment
- Flexible work arrangements (remote/hybrid options available)
- Professional equipment allowance to ensure you have the tools you need to perform at your best
- Professional development courses allowance to support continuous learning and career growth
- A diverse, international team shaping the future of destinations
Research Officer – Climate Change Mitigation Research Programme
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Inland Fisheries Ireland (IFI) has an exciting opportunity for an Research Officer Climate Change Mitigation to join the Research and Development division.
The Research officer will be responsible for day to day delivery of IFI's climate change mitigation research programme (CCMRP). He/she will be responsible for providing high quality scientific data to support management, conservation and protection of fish species and their habitats for climate change amelioration. The broad objective of the programme is to build an evidence based research programme to assess the impact of climate change on the Irish fisheries sector in both freshwater and estuarine environments.
The successful candidate will have demonstrated an excellence in planning and execution of applied scientific studies in field situations. The work will involve both desk and field investigations. The appointee will produce detailed scientific reports and papers on the progress of the project.
ABOUT US
Inland Fisheries Ireland are the environmental agency responsible for protecting, managing and conserving Ireland's inland fisheries and sea angling resources.
More information can be found by visiting our website.
VISION, MISSION & VALUES
Vision
To place the inland fisheries resource in the best sustainable position possible for the benefit of future generations.
Mission
To protect, manage and conserve Ireland's inland fisheries and sea angling resources and to maximise their sustainability and natural biodiversity.
Values
- We work collaboratively with professionalism
- We are open, transparent and accountable
- We act with respect and integrity
- We are committed to stewardship and sustainability
The Research Officer will be required to:
Main duties will include:
- Day to day delivery of the project under the supervision of the senior research officer.
- Working with the Senior Research Officer to develop a comprehensive and innovative research programme to examine climate change impacts on fish species and their habitats in Ireland.
Management
- Manage, coach, mentor, train and motivate staff
- Account management and monitoring to ensure programme is completed within the allocated budget, including reporting on a monthly basis
- Tendering and procurement of equipment.
- Provision of task schedules for all survey work.
- Compile standard operating procedures (SOPs) for any new work activities.
Research
- Undertake innovative research to bridge a significant knowledge gap related to Ireland's fish species and their habitats and climate change impacts in freshwater and Earnestine ecosystems.
Data Collection Responsibilities
- Collect data on fish populations (distribution, biology and ecology) and relevant environmental and abiotic data from designated water bodies as part of a long-term monitoring network.
- Supervise, prepare, install and maintain new or existing technologies where appropriate to support the programme.
- Develop/refine appropriate sampling methods in line with best practice.
Data Processing
- Data mining, data processing, collation and aggregation of all datasets and all sample materials to parameterize and validate models and or analyses.
- Quality assure and review all datasets for entry to databases/GIS. Maintain raw data and all other records in a clear concise manner and in line with IFI's database structure.
Data analysis
- Supervise and undertake data analysis of all relevant datasets, including using relevant statistical/modelling techniques.
- Liaise with GIS team to calculate landscape coviariates and develop vulnerability maps, etc.
- Develop models to predict the impacts of climate change associated changes in temperature and other parameters on Irish fish species and their habitats
Reporting
- Collate and write reports and scientific publications where necessary to agreed deadlines.
- Provision of weekly and monthly updates to the programme manager.
Other Duties
- Carry out such duties as may be assigned to the post from time to time by the Senior Research Officer.
- Ensure that all elements of the programme are achieved in a timely and efficient manner.
- Demonstrable capacity to communicate positively and effectively with internal and external stakeholders
Note: The above attempts to outline in a broad sense the range of duties associated with the Research Officer post. However other duties may arise as the requirements of the project and our stakeholders change over time.
The ideal candidate must, on or before the closing date have the following;
KEY EXPERIENCE & QUALIFICATIONS
Essential:
- A primary degree in relevant area (e.g. aquatic ecology, fisheries, fluvial geography)
- Circa 5 years' experience in working at a professional level in relevant area
- Full driving licence valid in the state
- Excellent inter-personal skills with particular emphasis on motivation and leadership and a proven track record of achieving objectives
- Excellent team working skills
- Self -directed and able to work independently
- Excellent attention to detail with the ability to spot errors and question information received
- Proven project management experience in a multi-disciplined team essential (including budgeting, scheduling, risk management, etc.)
- Demonstrable experience in report and scientific writing
- Demonstrable experience of field survey and data collection in aquatic habitats.
- Demonstrable experience in sampling and identification of fish species.
- A strong expertise in IT skills is required (GIS Software in addition to MS Office skills).
- Demonstrable experience in the use of relevant statistical software (e.g. R package).
- Knowledge of climate change and the potential impacts on Ireland's fish species.
- Experience in planning, executing and reporting on original research studies.
- The position will require flexibility regarding working hours.
Desirable Selection criteria:
- Postgraduate qualification in relevant area
- Demonstrable experience and good knowledge of at least one of the following areas: spatial modelling; fish habitat modelling; spatial stream network models; fish habitat suitability models; environmental flows; analysing/modelling time series or spatial data; acoustic telemetry)
- Full EB driving licence
- Published at least two scientific papers as first author in a relevant scientific field
- Experience in using remote technology (e.g. temperature loggers, data buoys, acoustic receivers, etc.).
Inland Fisheries Ireland is an equal opportunities employer
LOCATION
The position is based in IFI's head office in Citywest, Dublin. However, there may be considerable travelling and residing in locations across Ireland, whilst conducting field work in all weather conditions. Travelling on a daily or weekly basis will be a requirement. Transport will be provided for field duties. The work will require frequent physical exertion while conducting field activities, including walking over rough, uneven terrain, lifting equipment, wading in streams/rivers and working in boats.
REMUNERATION
The salary scale for the position is at the level of Research Officer applies in Inland Fisheries Ireland, it is a 14-point scale:
Point 1 €47,483.07; Point 2 €9,607.72; Point 3 ,690.22; Point 4 ,349.17; Point 5 57,575.81; Point 6 ,751.09; Point 7 ,710.66; Point 8 ,060.46; Point 9 9,536.49; Point 10 ,007.53; Point 11 ,466.07; Point 12 ,957.10; Point 13(LSI 1) ,785.70; Point 14(LSI 2) ,372.97 (IFI Research Officer Grade Pay Scale as of
Candidates should note that salary will not be subject to negotiation and the rate of remuneration may be adjusted from time to time in line with Government pay policy. New entrants to the public sector will start on point 1 subject to Haddington Road Agreement and subsequent Government Agreements.
TENURE
This post is externally funded until 31st July 2026 and offered on a Specified Purpose Contract.
APPLICATIONS & SELECTION PROCESS
A cover letter and up to date Curriculum Vitae) should be submitted by 5.00 pm Wednesday on the 1st of October 2025.
Late applications will not be processed.
Short listing will be based on information provided in the Cover Letter and CV.
Canvassing will disqualify.
Inland Fisheries Ireland is an equal opportunities employer.
FORMATION OF PANEL
A panel may be created for up to six months to cover vacancies for roles with similar skill sets.
Inland Fisheries Ireland is an equal opportunities employer
Clinical Research Specialist
Posted today
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About Teckro
We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
Could you be our newest Teckronaut?
What you'll Do:
- Responsible for the training, mentoring and development of CRS Level 1, including the preparation and development of training materials and tools
- Assisting with the updating of clinical operations process guides
- Responsible for quality checking previously developed projects as part of risk assessment
- Involved in the assessment of client documents prior to project development to determine project timelines
- As delegated, will assist in the planning and backlog of projects
- Analyse, understand, and process complex scientific/medical/pharmaceutical information
- Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
- Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
- Monitor, analyze, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
- Successfully complete the 'In-House Clinical Trial Training Programme' delivered by a Senior CRS, covering all aspects of Clinical Trials, including but not limited to: trial design, trial procedures, ICH-GCP, clinical trial regulations, operational activities, safety reporting, monitoring etc. The CRS Level 2 will be deemed competent by both the Senior CRS and CRS Manager.
- Undertake other duties in-line with your role and business requirements as required
Multilingual CRS:
- Assist with translation tasks across various departments within the company
- To perform study demos of Teckro, to join Investigator's Meetings (IMs) and to provide training in local languages to study teams and/or relevant users
The Ideal candidate will have:
- Japanese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking.
- Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.
- Superb editorial skills with a keen eye for text and graphic layouts
- Strong critical thinking and problem solving skills
- Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
- Strong interpersonal, verbal and written communication skills
- Superb editorial skills with a keen eye for text and graphic layouts
- Proven ability to organize information in a logical and systematic way
- Ability to focus on fine details and the wider system at the same time
- Extreme attention to detail and accuracy even when balancing multiple projects
- Highly adaptable and flexible
- Ability to quickly and easily switch contexts, particularly between creative and analytical work
- Passion for creative solutions, innovation, and divergent thinking
- Demonstrated ability to work well as part of a team
- Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential
Qualifications Required:
- At least 18+ months relevant experience with proven competencies in the role.
- Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
- Excellent computer skills
Location and Travel:
(Dublin)
- Hybrid role - Dublin City Centre, Ireland.
- Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
- We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
- Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.
Teckro Benefits:
- 25 days holidays
- Pension
- Healthcare
- Life Insurance
- Share Options
- 50% Maternity leave pay after capped length of service
- Paid Paternity leave scheme
- Bike to Work/ Tax Saver Scheme
- Gym/Wellness Allowance
- Sports and Social Club
We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you
By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.
Research Internship – Security
Posted today
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Introduction
IBM Research Scientists are charting the future of Artificial Intelligence, creating breakthroughs in quantum computing, discovering how blockchain will reshape the enterprise, and much more. Join a team that is dedicated to applying science to some of today's most complex challenges, whether it's discovering a new way for doctors to help patients, teaming with environmentalists to clean up our waterways or enabling retailers to personalize customer service.
Your Role And Responsibilities
At the Dublin Research Lab, in the Security teamwe focus primarily on the Security and Privacy ofGenAI. From research to product, we are interested in scientific contributions to the field, as well as real world innovative solutions. Currently we have varied internship opportunities across the area.
We would like to talk to people with a general interest in the security of generative AI. This includes model hardening approaches through curated data sets and advanced fine-tuning approaches, via e.g. differential privacy. Prompt inspection for security threats. Model output analysis to ascertain levels of sensitive information leakage etc. The internship will aim for publications in top-tier conferences, NeurIPS, AAAI, ICML, etc.
Preferred Education
Master's Degree
Required Technical And Professional Expertise
- Working knowledge in deep learningand familiarity with NLP.
- Strong Python programming skills
- Experience of working with deep learning libraries, e.g. TensorFlow, Pytorch, Keras and NLP tools, e.g. NLTK, Transformers, spaCy.
- Solid understanding of mathematical concepts such as probabilities, statistics and linear algebra.
Preferred Technical And Professional Experience
N/A
Clinical Research Specialist
Posted today
Job Viewed
Job Description
About Teckro
We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
Could you be our newest Teckronaut?
What you'll Do:
- Responsible for the training, mentoring and development of CRS Level 1, including the preparation and development of training materials and tools
- Assisting with the updating of clinical operations process guides
- Responsible for quality checking previously developed projects as part of risk assessment
- Involved in the assessment of client documents prior to project development to determine project timelines
- As delegated, will assist in the planning and backlog of projects
- Analyse, understand, and process complex scientific/medical/pharmaceutical information
- Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
- Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
- Monitor, analyze, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
- Successfully complete the 'In-House Clinical Trial Training Programme' delivered by a Senior CRS, covering all aspects of Clinical Trials, including but not limited to: trial design, trial procedures, ICH-GCP, clinical trial regulations, operational activities, safety reporting, monitoring etc. The CRS Level 2 will be deemed competent by both the Senior CRS and CRS Manager.
- Undertake other duties in-line with your role and business requirements as required
Multilingual CRS:
- Assist with translation tasks across various departments within the company
- To perform study demos of Teckro, to join Investigator's Meetings (IMs) and to provide training in local languages to study teams and/or relevant users
The Ideal candidate will have:
Chinese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking.
Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.
Superb editorial skills with a keen eye for text and graphic layouts
Strong critical thinking and problem solving skills
- Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
- Strong interpersonal, verbal and written communication skills
- Superb editorial skills with a keen eye for text and graphic layouts
- Proven ability to organize information in a logical and systematic way
- Ability to focus on fine details and the wider system at the same time
- Extreme attention to detail and accuracy even when balancing multiple projects
- Highly adaptable and flexible
Ability to quickly and easily switch contexts, particularly between creative and analytical work
Passion for creative solutions, innovation, and divergent thinking
Demonstrated ability to work well as part of a team
- Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential
Qualifications Required:
- At least 18+ months relevant experience with proven competencies in the role.
- Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
- Excellent computer skills
Location and Travel:
(Dublin)
- Hybrid role - Dublin City Centre, Ireland.
- Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
- We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
- Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.
Teckro Benefits:
- 25 days holidays
- Pension
- Healthcare
- Life Insurance
- Share Options
- 50% Maternity leave pay after capped length of service
- Paid Paternity leave scheme
- Bike to Work/ Tax Saver Scheme
- Gym/Wellness Allowance
- Sports and Social Club
We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you
By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.
Clinical Research Nurse
Posted today
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We are looking for a new research nurse to cover maternal leave to join our operation in Tallaght hospital. Experience of clinical research is preferable, but not essential.
The initial contract will be fixed term for around 6-9 months, but there is a good possibility that the role will become permanent after this, but we cannot guarantee this at this stage.
MAIN PURPOSE:
The research nurse will play a pivotal role in the coordination of clinical trials. Under the supervision of the research manager the post holder will be involved in executing all activities relating to the clinical studies, ensuring compliance with regulatory requirements.
MAIN DUTIES AND RESPONSIBILITIES:
Research responsibilities will include
· Working within CRP standard operating procedures and research protocols/plans ensuring the overall smooth running of clinical trials/Investigations in accordance with Good Clinical Practice (GCP) and applicable regulatory and ethical requirements.
· Study Coordination and management of multiple research projects
· Screening of patients to identify potential study candidates, evaluation and enrolment of suitable participants in clinical research trials/investigations under the direction and supervision of the Principal Investigator (PI).
· Management and accountability for Investigational Medicinal Product/Device (IMP/IMD)
· Playing a proactive role in driving on-going clinical research projects through participant recruitment, participant follow-ups, safety reporting, early identification of potential problems and regular feedback with Principal Investigator and research team.
· Ensuring the maintenance and upkeep of clinical research documentation, including site files, case record forms, monitoring arrangements, data correction, data collection and data entry as per GCP/protocol and data protection requirements.
· Ensuring prompt management of all study related correspondence.
· Ensuring research data is accurate and verifiable and is collected, stored and handled on site in compliance with the protocol and data protection requirements
· Preparation for and participation in monitoring visits and Internal/Sponsor/Regulatory audit/inspection as required
· Development and maintenance of strong relationships with research partners, key stakeholders and team members by acting as the first point of contact on a variety of research projects and liaising with project collaborators, stakeholders, and staff.
· Playing a pivotal role in educating relevant research and clinical staff on current and upcoming clinical trials/investigations
Clinical Practice responsibilities will include:
· Provide nursing knowledge, expertise and care to patients participating in a clinical trial. Ensure that patients are fully informed of all details pertaining to the clinical trial/research project prior to their recruitment as per GCP.
· Ensure patients understand their disease and the proposed research and standard treatment options.
· Attend out-patient clinics for the purpose of optimising patient recruitment to clinical research studies.
· Maintain competence in the area of relevant national and European standards including data privacy and ethical standards and regulations
· Ensure competence/training in all designated research activities prior to carrying out such activities on research participants
· Performs study procedures (e.g., Administration of IP. Oral, SC, IM, monitoring of infusions, Phlebotomy, obtain and process biological specimen samples, obtain ECG recordings, vital signs, Spirometry and safety assessments) as required by study protocol under the supervision of the Principal Investigator (PI)
· Ensure continuity of patient care by liaising with outside health care professionals, and those who are involved in clinical work where applicable.
· Use agreed processes to deal with referrals and enquiries from other hospitals
· Carry out other duties as appropriate to the post as may be assigned from time to time by line manager/CRP management team
Professional development
· Maintain professional registration
· Take responsibility for own professional development and skills updating including maintaining a record of training activities and experience gained.
· Work with PI and CRP management team to ensure the safe delivery of care to patient participating in the clinical study
· Work closely with CRP's Management to ensure that appropriate quality documentation and performance measures are in place for improved processes.
The post holder requires
· Degree in Nursing and a minimum of 3 years' nursing experience
· Current registration with the Nursing and Midwifery Board of Ireland (NMBI)
· Proven clinical skills such as basic life support training and ability to provide safe and high-quality nursing care to a wide variety of research participants across different disease spectrums.
· Excellent oral and written communication skills.
· Good organizational, analytical/critical thinking and problem-solving skills with an ability to prioritize tasks/workload and meet deadlines
· Evidence of accuracy and attention to detail
· Knowledge of Microsoft office applications and willingness to develop computer skills further
· Knowledge of relevant data protection requirements
· Understanding of Good Clinical Practice
· Ability to work autonomously or as part of a team and to demonstrate initiative.
It would be desirable that post holder would have:
· Have experience of working on clinical trials or within a research setting
· Be competent in phlebotomy procedures
· Biological sample handling and processing experience with IATA certification
Job Types: Full-time, Fixed term
Pay: €40,000.00-€56,000.00 per year
Education:
- Bachelor's (required)
Work Location: In person
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Clinical Research Specialist
Posted today
Job Viewed
Job Description
About Teckro
We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
Could you be our newest Teckronaut?
What you'll Do:
- Responsible for the training, mentoring and development of CRS Level 1, including the preparation and development of training materials and tools
- Assisting with the updating of clinical operations process guides
- Responsible for quality checking previously developed projects as part of risk assessment
- Involved in the assessment of client documents prior to project development to determine project timelines
- As delegated, will assist in the planning and backlog of projects
- Analyse, understand, and process complex scientific/medical/pharmaceutical information
- Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
- Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
- Monitor, analyze, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
- Successfully complete the 'In-House Clinical Trial Training Programme' delivered by a Senior CRS, covering all aspects of Clinical Trials, including but not limited to: trial design, trial procedures, ICH-GCP, clinical trial regulations, operational activities, safety reporting, monitoring etc. The CRS Level 2 will be deemed competent by both the Senior CRS and CRS Manager.
- Undertake other duties in-line with your role and business requirements as required
Multilingual CRS:
- Assist with translation tasks across various departments within the company
- To perform study demos of Teckro, to join Investigator's Meetings (IMs) and to provide training in local languages to study teams and/or relevant users
The Ideal candidate will have:
- Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.
Superb editorial skills with a keen eye for text and graphic layouts
Strong critical thinking and problem solving skills
- Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
- Strong interpersonal, verbal and written communication skills
- Superb editorial skills with a keen eye for text and graphic layouts
- Proven ability to organize information in a logical and systematic way
- Ability to focus on fine details and the wider system at the same time
- Extreme attention to detail and accuracy even when balancing multiple projects
- Highly adaptable and flexible
Ability to quickly and easily switch contexts, particularly between creative and analytical work
Passion for creative solutions, innovation, and divergent thinking
Demonstrated ability to work well as part of a team
- Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential
Qualifications Required:
- At least 18+ months relevant experience with proven competencies in the role.
- Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
- Excellent computer skills
Location and Travel:
(Dublin)
- Hybrid role - Dublin City Centre, Ireland.
- Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
- We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
- Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.
Teckro Benefits:
- 25 days holidays
- Pension
- Healthcare
- Life Insurance
- Share Options
- 50% Maternity leave pay after capped length of service
- Paid Paternity leave scheme
- Bike to Work/ Tax Saver Scheme
- Gym/Wellness Allowance
- Sports and Social Club
We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you
By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.
Research Impact Manager
Posted today
Job Viewed
Job Description
About Taighde Eireann - Research Ireland
Taighde Eireann - Research Ireland is the national research and innovation funding agency which was established on 1 August 2024; it amalgamates the activities of the Irish Research Council and Science Foundation Ireland. Research Ireland will drive world class research and innovation in Ireland, funding research and innovation excellence in all disciplines across the spectrum of Arts, Engineering, Humanities, Mathematics, Science, Social Sciences, Technology, and others. We believe in the power of research to create a better future for society, economy, and the environment in Ireland, and that research can be truly impactful when it is shaped and informed by the society it serves.
The Research for Society Directorate leads on programmes that fund individual-led research grants for researchers at all career stages, international partnership programmes and PhD training programmes. It also leads on the development and delivery of a suite of challenge-based funding initiatives, including the EU-funded 'National Challenge Fund' , and also leads on the Public Service Fellowship, forging researcher-policymaker collaboration. In addition, it leads on the delivery of a broad portfolio of Education and Public Engagement initiatives and funding calls, including flagship activities such as Science Week.
We are now recruiting for a Research Impact Manager to join 'Research for Society' on a 4-year FTC basis. This represents an exciting career opportunity for a suitably qualified individual to lead and influence and highly ambitious, innovative, and potentially high impact research programmes. As an impact specialist you will play a critical role in the delivery of Research Ireland's mission, particularly in supporting the delivery of the National Challenge Fund.
About the Role
Research Ireland is dedicated to supporting researchers to develop solutions to complex societal challenges. In recent years, we have developed novel approaches to supporting research teams through challenge-based or mission-oriented initiatives. Challenge-based funding supports ambitious, highly motivated innovators to address society's most significant challenges, delivering tangible benefits over well-defined timeframes. Challenge-based funding programmes enable research teams to contribute to solving challenges of strategic national importance, thereby sustaining and growing Ireland's competitiveness, but also providing our community with support to mobilise action on global issues.
The Research Ireland Challenge Team is responsible for the development and implementation of a suite of challenge-based funding programmes including the large scale 'National Challenge Fund', funded under the EU Recovery and Resilience facility and through multiple partnerships with Government bodies including with Irish Aid under the Sustainable Development Goals Challenge and with the Defence Forces under the DefOrg Innovation challenge. Through these and other approaches, the team is responsible for providing additional supports in areas such as Theory of Change, Design Thinking, and Impact Pathway development.
Challenge funding represents an approach to engaged research, which recognises that to address complex societal challenges, stakeholders, beneficiaries, and end-users should be involved in the cocreation of research activities and should inform the expected outputs and outcomes to ensure that they are meaningful and relevant. The Translational Specialist will develop and implement ways to support research teams in new ways to maximise the translation of research and solutions to society. This position plays a key part in ensuring the delivery of impactful initiatives that align with the organisation's overarching mission.
Key Responsibilities
- Identify and develop opportunities to support research teams to translate their work into impactful applications through for example, policy, commercialisation, and social innovation.
- Design, develop and deliver initiatives and interventions to facilitate Challenge Teams enhancing the impact of their research.
- Assess the effectiveness of impact initiatives and implement plans for continuous improvement.
- Contribute to broader organisational goals by identifying opportunities to collaborate, synergise, and support other teams with research impact and commercialisation.
- Stay at the cutting edge of global best practices in impactful research and integrate emerging trends and technologies into Research Ireland initiatives.
- Build strong relationships with researchers, stakeholders, and policymakers to enhance the reach and impact of Research Ireland initiatives.
- Support the design, execution, monitoring and evaluation of Challenge Funding initiatives, ensuring alignment with organisational goals, requirements of partners and funders, and value for money.
- Act as spokesperson and representative for Research Ireland in national and international fora, as required.
Essential Criteria
- Hold a third-level qualification (PhD, MBA, Masters) in a relevant discipline.
- At least 10 years of relevant experience, ideally in translational research, research commercialisation, entrepreneurship, or a relevant related impact area.
- Proven experience in developing and implementing impact strategies within a relevant sector, such as research or technology.
- Demonstrated ability to work at a strategic level yet also drive daily execution.
- Have proven analytical, problem-solving, and interpretive skills with an ability to think strategically and use sound judgement on complex issues.
- Be well-organised with the ability to multitask, prioritise, meet deadlines, and manage competing and changing priorities in a dynamic environment.
- Proven experience in building and maintaining high-level relationships with diverse stakeholders, including researchers, policy-makers, investors, and entrepreneurs.
- Exceptional written and verbal communication skills, with the ability to present information in a confident, logical, and convincing manner.
- Ability to measure impact, evaluate interventions, and provide insights to inform strategic decision-making.
- Have a professional, positive, and enthusiastic attitude, aligned to delivering the objectives and goals of Research Ireland.
- Ability to work well under pressure, demonstrating integrity, energy, and resilience.
Desirable Criteria
- Experience of working with, and developing, teams
- Hands-on experience of research commercialisation
- Experience in managing budgets
- Experience working in an impact or solution-oriented environment
- Understanding of the challenges and opportunities in translating research into practical applications.
- Experience in working within multi-/interdisciplinary research environments.
Key Competencies
- Ability to develop and articulate a long-term vision that aligns with organisational goals
- Leadership in a dynamic environment, managing competing priorities
- Management and delivery of results
- Supporting team professional development
- Initiative and creativity
- Ability to influence and advocate effectively within and beyond the organisation
- Advanced interpersonal and communication skills
Application Process:
To apply for this post, applicants must submit a cover letter demonstrating how the applicant meets the requirement for this role (maximum of two pages) as set out in the job specification together with an up-to-date CV in one document.
Please note that the cover letter is essential and candidates will be rejected for not including one.
Applications must be submitted as one document online through the online applicant management system Occupop on or before 12 noon Irish Local Time on 26th September 2025.
Shortlisted applicants will be invited to attend for an interview, which may include a competency-based interview, a presentation on a topic of relevance to the role and/ or other such assessment methods as deemed appropriate.
Research Ireland reserves the right to invite candidates to a second-round interview and to undergo further assessment, including the use of psychometric assessment if so required. Please note, interviews may take place over videoconference or other remote technology where appropriate.
Salary
This role will be appointed at Level E, €81,475 to €100,064 per annum plus contributory superannuation pension. Please note that Government policy continues to be that starting pay on recruitment from open competition for all posts within the public service should be at the minimum of the relevant salary scale and are not subject to negotiation.
Please note that new entrants to the public sector will be appointed at the minimum point of the salary scale. Remuneration may be adjusted from time to time in line with Government policy.
Benefits
- 30 days annual leave per annum, (+ 1 Organisation holiday day + 10 additional public holidays = 41 days).
- Defined Benefit Pension Scheme (Single Public Service Scheme)
- Favourable Hybrid / Blended working policy for employees.
- Subsidised canteen.
- Long term illness income protection
Additional information
The role will be based in the Research Ireland office located in Three Park Place, Hatch Street Upper, Dublin 2, Ireland, D02 FX65, but travel around Ireland will be required on a regular basis. Research Ireland currently operates a hybrid/flexible working model.
For this role, a minimum of two days a week in the office is required, in addition to nationwide travel as required for business needs.
Research Ireland is an equal opportunities employer and is committed to fostering an inclusive workplace which values and benefits from the diversity of our workforce. We encourage you to reach out to us directly at should you require assistance or reasonable accommodation during the recruitment process with Research Ireland.
Clinical Research Associate
Posted 4 days ago
Job Viewed
Job Description
At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
**POSITION SUMMARY:**
Assist in the clinical trial management to ensure timelines and metrics are met and maintained throughout the study. Provides support in the oversight and management of vendors. Conducts review of clinical data to ensure site adherence to applicable regulatory requirements, International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Good Clinical Practice (GCP) Guidelines, company standard operating procedures (SOPs), and study protocol.
**KEY RESPONSIBILITIES:**
+ Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH GCP Guidelines, company SOPs, and study protocols. Ensure timelines and metrics are met and maintained throughout the study.
+ Has a good knowledge of the therapeutic area and product.
+ Obtains a complete understanding of all trial-related documents and operational procedures with moderate direct supervision
**Audits/Inspections/Quality Assurance (QA):**
+ Supports with effective and timely audit/inspection responses.
**Clinical Trial Design/Performance:**
+ Gains exposure/participates in case report form (CRF) development, interactive "X" recognition system (IXRS) set-up, central laboratory (lab) set-up, and other vendor selection processes and is capable of training others.
+ Oversees completion of Pre-Study Visits (PSVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs), to determine protocol and regulatory compliance.
+ Contributes to the resolution of escalated issues from study centers, regulatory authorities and institutional review board (IRBs)/independent ethics committees (IECs) with the support of the supervisor, if needed.
+ Performs Sponsor Site Visits at selected sites to demonstrate oversight of the monitoring process and documenting the visits in the Sponsor Site Visit Report.
+ Oversees study centers to ensure timely execution of the clinical studies, generating quality data ensuring the well-being of the study subjects and the trial integrity with moderate supervision.
+ With the support from the supervisor, may support in the creation, review and tracking of study documents.
+ May assist on the TMF reviews and resolution of findings, internally or interacting with the CRO with support if needed.
**Clinical Trial Materials (CTM):**
+ Provides support on the regulatory document review and approval for investigational product (IP) release.
+ Provides support in clinical product technical complaints and product recall as necessary.
+ Provides support and information to the CTM staff regarding IP management, as needed.
**In-house Monitoring:**
+ May assists with expedited identification, retrieval, and review of study documents particularly those required for site activation/study start-up.
+ May facilitate investigator site payments, as applicable.
**Management/Training Team** :
+ Ability to facilitate meetings (e.g. Investigator Meetings, Kick-off meetings).
+ May provide support for the monitor training and contribute to resolve the issues they identified.
+ Collaborates in ensuring that appropriate training is conducted for CRO staff, vendors, investigators, and study site staff on study requirements and internal SOPs (if applicable).
**Monitoring:**
+ Reviews and tracks comments of monitoring reports generated by the vendor (i.e. CRO) as part of Sponsor Oversight of Vendor Clinical Site Monitoring activities.
+ With the support of the supervisor, if needed, verifies study documents (e.g., case report forms, source documents, adverse events) are tracked and reviewed for completeness and accuracy to ensure data integrity.
+ Tracks study specific tasks and progress of the trial.
+ Gets more insight, maintains and updates clinical trial management system (CTMS) information pertaining to the study.
+ Is involved in the oversight of vendor clinical monitoring activities. Ensures that the clinical monitoring process is done in adherence to an international ethical and scientific quality standard to provide public assurance that the clinical data are credible.
+ May collaborates with data management to resolve queries.
**Vendor Management:**
+ Assists in the management of vendor performance during conduct of the study with moderate direct supervision.
+ Assists in evaluation of vendor performance during conduct of the study.
+ Reviews/creates/tracks trial newsletters, memos, mass correspondence, or other appropriate trial-related documentation, with moderate supervision.
+ Facilitates the scheduling of internal team meetings, cooperating with defining the agenda and creating the meeting minutes, if needed.Additional On-site Monitoring Responsibilities:
**In-house Monitoring:**
+ Performs monitoring/co-monitoring activities for site initiation visits, interim site monitoring, and closeout visits, in conformance to all relevant laws, regulations, guidelines and internal SOPs/policies.
+ Identifies/screens/qualifies investigators through feasibility questionnaires and pre-study visits.
+ Reconciles clinical supplies and drug accountability records at study sites.
+ Verifies study documents (e.g., case report forms, source documents, adverse events) are tracked and reviewed for completeness and accuracy to ensure data integrity.
+ Identifies and effectively documents site findings with an equal ability to re-train, place corrective action in place with the site, and follow-up as required.
+ Reviews, clarifies, and obtains, data changes via query resolutions with site personnel.
+ Conducts completion of PSVs, SIVs, IMVs, and COVs, to determine protocol and regulatory compliance.
+ Prepares telephone contact reports, confirmation letters, site visit reports (PSV, SIV, IMV, and COV), and follow-up letters to accurately and completely document site status and activities in agreement with the Clinical Monitoring Plan for the study.
**Monitoring:**
+ Assists with expedited identification, retrieval, and review of study documents particularly those required for site activation/study start-up.Safety:
+ Understands and supports implements processes for distribution and tracking of SAE's, safety documentation, and pregnancies. Monitors compliance of these processes.
**PERSON SPECIFICATION**
+ Typically requires 2 years of experience in clinical research, including a minimum of 1-year field monitoring experience (e.g., independent monitoring, co-monitoring, accompanied site visits).
+ Associate's degree in a life science field required.
+ Relevant experience in clinical research and field monitoring experience preferred (e.g. independent field monitoring and co-monitoring).
+ 4 years clinical research experience with 2 years experience as a CRA
+ Bachelor's degree or higher degree in a life science field preferred.
**Our Benefits Include:**
+ Highly competitive salary
+ Group pension scheme - Contribution rates are (1.5% / 3%/ 5%/ 7%) and company will match
+ Private Medical Insurance for the employee (Irish Life)
+ Ongoing opportunities for career development in a rapidly expanding work environment
+ Succession planning and internal promotions
+ Education allowance
+ Wellness activities - Social activities eg. Padel, Summer Events
We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply - we're excited to hear from you
#LI-FD1
Learn more about Grifols ( ID:**
**Type:** Regular Full-Time
**Job Category:**