36 Research Assistants jobs in Ireland

12 Months, Specific Purpose, Whole-Time Post Position Summary Are you a qualified nurse, looking for an impactful role that involves helping patients whose lives have been impacted by cancer? Do you want to join a passionate and growing team with recent funding from the Breast Cancer Research Foundation to grow and find better diagnostics and treatments for patients with breast cancer? The UCC Cancer Trials Group (UCC CTG) is looking for an enthusiastic research nurse (CNMII) to work in a growing team, supporting investigator-led research. ABOUT UCC CTG: The UCC CTG is a new HRB funded collaborative team which aims to bring together a dedicated team of cancer specialists and research staff across the south of Ireland. The UCC CTG is part of Cancer Research @UCC, a translational cancer research centre within the College of Medicine & Health at University College Cork. The UCC CTG group includes 3 cancer trials units at Cork University Hospital (CTC @CUH), University Hospital Waterford and Bons Secours Hospital Cork. For more information about the group, check our website: or our Twitter @UCCCancerTrials ABOUT ACADEMIC RESEARCH AT CTC @CUH: The role will be hosted in Cancer Research @UCC and the Cancer Trials Cork Unit at CUH (CTC @CUH) in the Breast Lung Gynaecology portfolio. The CUH unit has been in operation for close to two decades, serving a geographically diverse population of 1.2 million in the South of Ireland. This team has grown over the past few years and continued growth is projected for years to come. The CNMII will work closely under the guidance of Professor Roisin Connolly /CNM3 /Nurse Management and team members. As a summary, the role will include: Co-ordination of clinical and translational aspects of the project including direct interface with pathology department, scientific collaborators, external laboratories and data scientists etc. Clinical responsibilities. Working with pathology for slide cutting and storage, labelling etc Coordination of sample distribution to labs and payments/invoices for correlative studies. Keeping accurate logs of the specimens and results, linking with Castor database (study database) where relevant Collection of clinical data from relevant databases when required for abstract preparation Supporting team meetings (minutes/agendas/follow up tasks) specific to the project Support other studies taking place in the Cancer Trials Cork unit at Cork University Hospital where deemed necessary and in keeping with funding requirements Engage cross-functionally with different stakeholders, knowledge sharing, and building relationships. This role requires excellent communication and interpersonal skills, computer literacy, organization and an awareness of time management. The MINA study - 'Microbiome Immunotherapy Neoadjuvant Assessment' - is a prospective observational study that aims to characterise and evaluate the bacterial population shown to be present in the immediate environment of breast tumours. Previous work has shown that these bacteria can alter the effectiveness of some commonly used anti-cancer drugs, and so it is hoped that data from this study can support the development of new biomarkers that can measure how well some patients might respond to chemotherapy compared to others. EXPERIENCE REQUIRED: Qualified Nurse (Mandatory RGN, BSc). Oncology background or related experience would be a strong advantage. Strong interest in gaining experience in this area will also be considered without previous experience in Oncology nursing. WAYS TO GET IN TOUCH: You can confidentially email queries to or Or apply with your CV through Type the job ID into the keywords section and the role will come up. Project Title: UCC Cancer Trials Group (Cancer Research @ UCC / Cancer Trials Cork @CUH) Post Duration: 12 Months Salary: €61,463 - €77,666 p.a (CNM2 salary scale) (As required by public pay policy for the higher education sector, new appointments to a direct entry recruitment grade will generally be at the minimum (1st point) of the relevant scale. For existing public servants, the restriction to the first point on scale may be varied where a person is appointed to the same or an analogous grade, role or position as their previous public service employment.) For an information package including further details of the post see Informal enquiries can be made in confidence to informal enquiries: to Prof. Roisin Connolly or Applications must be submitted online via the University College Cork vacancy portal Queries relating to the online application process should be referred to quoting the job-title and project name. Candidates should apply, in confidence, before 12 noon (Irish Local Time) on Friday 17th October 2025. No late applications will be accepted. Please note that an appointment to posts advertised will be dependent on University approval, together with the terms of the employment control framework for the higher education sector. UCC is committed to creating and fully embracing an inclusive environment where diversity is celebrated. As a University we strive to create a workplace that reflects the diversity of our student population where people from a wide variety of backgrounds learn from one another, share ideas, and work collaboratively. UCC is committed to being an employer that recognises the value of diversity amongst its staff. We encourage applicants to consult our policies at and initiatives at and we welcome applications from everyone, including those who are underrepresented in the protected characteristics set out in our Equal Opportunities & Diversity Policy. UNIVERSITY COLLEGE CORK IS AN EQUAL OPPORTUNITIES EMPLOYER To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

12 Months, Specific Purpose, Part-Time Post Position Summary Are you a qualified nurse, looking for an impactful role that involves helping patients whose lives have been impacted by cancer? Do you want to join a passionate and growing team in cancer research at Cork University Hospital? The UCC Cancer Trials Group (UCC CTG) is looking for an enthusiastic research nurse (Clinical Nurse Manager 1) NMBI registration required 19.5hrs a week or part time to support the cancer trials team at Cork University Hospital - Cancer Trials Cork Unit. ABOUT UCC CTG: The UCC CTG is a new HRB funded collaborative team which aims to bring together a dedicated team of cancer specialists and research staff across the south of Ireland. The UCC CTG is part of Cancer Research @UCC, a translational cancer research centre within the College of Medicine & Health at University College Cork. The UCC CTG group includes 3 cancer trials units at Cork University Hospital (CTC @CUH), University Hospital Waterford and Bons Secours Hospital more information about the group, check our website: or our Twitter @UCCCancerTrials ABOUT CANCER TRIALS CORK @CUH UNIT: Cancer Trials Cork @CUH has been in operation for close to two decades, serving a geographically diverse population of 1.2 million in the South of Ireland. Our broad portfolio encompasses phase 1-3 therapeutic trials in haematologic/solid malignancies, radiation therapy and surgery: including academic collaborative trials via Cancer Trials Ireland, and industry trials, with a developing portfolio of investigator-initiated trials (IITs). As a summary, the role will include (see more information in the candidate pack): Significant clinical responsibilities. Take part in portfolio studies taking place in the Cancer Trials Cork unit at Cork University Hospital. Engage cross-functionally with different stakeholders, knowledge sharing, and building relationships. This role requires excellent communication and interpersonal skills, computer literacy, organization and an awareness of time management. EXPERIENCE REQUIRED: Qualified Nurse (Mandatory RGN, BSc,). Oncology background or related experience would be a strong advantage. Strong interest in gaining experience in this area will also be considered without previous experience in Oncology nursing. Project Title: UCC Cancer Trials Group (Cancer Research @ UCC / Cancer Trials Cork @CUH) Post Duration: 12 Months Salary: €56,642 - €66,705 (pro rata 0.5 FTE) CNM1 scale (As required by public pay policy for the higher education sector, new appointments to a direct entry recruitment grade will generally be at the minimum (1st point) of the relevant scale. For existing public servants, the restriction to the first point on scale may be varied where a person is appointed to the same or an analogous grade, role or position as their previous public service employment.) For an information package including further details of the post see Informal enquiries can be made in confidence to informal enquiries: to Dr. Laia Raigal, Cancer Trials Group. Email: , or Applications must be submitted online via the University College Cork vacancy portal Queries relating to the online application process should be referred to quoting the job-title and project name. Candidates should apply, in confidence, before 12 noon (Irish Local Time) on Friday 17th of October 2025. No late applications will be accepted. Please note that an appointment to posts advertised will be dependent on University approval, together with the terms of the employment control framework for the higher education sector. UCC is committed to creating and fully embracing an inclusive environment where diversity is celebrated. As a University we strive to create a workplace that reflects the diversity of our student population where people from a wide variety of backgrounds learn from one another, share ideas, and work collaboratively. UCC is committed to being an employer that recognises the value of diversity amongst its staff. We encourage applicants to consult our policies at and initiatives at and we welcome applications from everyone, including those who are underrepresented in the protected characteristics set out in our Equal Opportunities & Diversity Policy. UNIVERSITY COLLEGE CORK IS AN EQUAL OPPORTUNITIES EMPLOYER To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Job Description Dunnes Stores is Ireland's leading retailer positioned at the cutting edge of food, fashion and home retailing. We have over 130 stores in Ireland, Northern Ireland and Spain, a strong e commerce business and are expanding our service and product offering all the time. We currently have a vacancy for a Research Analyst to join our team. This role is based full time in our Head Office in Dublin City Centre. Role Overview: We are seeking a Research Analyst to support the delivery of customer-focused qualitative research projects. Working within a dynamic retail insights team, you will help bring the voice of the customer to the forefront of business decision-making. This is an exciting opportunity for someone passionate about customer experience, behavioural research, and qualitative methodologies in a commercial context. You will be hands-on in managing research logistics, coordinating participant recruitment, hosting sessions, and capturing actionable insights that inform everything from product development to in-store experience. Key Responsibilities: Customer Recruitment & Session Management Recruit research participants from internal customer panels for live qualitative research, both in-person and online. Pre-screen and schedule participants to ensure the right fit for each project's objectives. Coordinate and run screener surveys using in-house survey tools. Host and attend research sessions, ensuring a smooth experience for participants and clients. Research Support & Execution Set up and manage session recording equipment (audio/video), including troubleshooting any tech-related issues on-site or remotely. Prepare discussion guides, stimulus materials, and session logistics as required. Take observational notes during sessions and provide assistance to moderators or third-party research agencies when applicable. Project Coordination & Logistics Provide operational and administrative support across multiple research projects simultaneously. Help manage timelines, booking venues, coordinating travel, and handling participant incentives. Travel to research locations across Ireland (and occasionally beyond), with flexibility to work outside regular hours when necessary (time off in lieu provided). Required Skills & Experience: Proven experience in a qualitative research commercial environment (agency, client-side) Comfortable working in a fast-paced and evolving Retail environment. Strong communication skills - articulate, approachable, and confident in engaging with both customers and stakeholders. Tech-savvy - capable of handling recording tools, video conferencing platforms, and survey software. Excellent attention to detail and organizational skills - able to manage multiple moving parts and adapt to changing priorities. Problem-solving mindset with the ability to stay calm under pressure and respond quickly to unforeseen challenges. A valid driver's license is required for travel to research sessions. Benefits: Competitive salary Comprehensive benefits package including our employee discount Opportunities for professional development and career progression A dynamic and collaborative work environment focused on innovation and growth If this sounds like the perfect job for you, please apply now and see what difference you could make! Dunnes Stores is an equal opportunity employer

Applications are now open for the position of Senior Research Funding Specialist (SRFS) within the Research Development Office (RDO), located in Trinity Research. The SRFS is a senior role, responsible for the design and delivery of a suite of professional supports to academic researchers and research groups, with the aim of increasing TCD participation and success in funded research programmes. The post holder will work within a central team of funding specialists, liaising closely with the wider network of research management and support professionals based in Schools and Centres, to deliver a coordinated and expert service to funding applicants. Senior Research Funding Specialists lead supports from the RDO on one or more funding programmes, managing a researcher-centred service, driving innovation in supports tailored to one or more grant types (fellowship, investigator, collaborative, commercialisation etc.) and bringing a broad disciplinary expertise to the team (e.g. health or life sciences, social sciences, arts/ humanities, physical or natural sciences etc.). Reporting to a Team Lead, the SRFS will contribute to TCD research funding success through agile leadership, teamwork and innovation in best practice supports to researchers. Note that three SRFS posts are available in the RDO at this time. Suitably qualified candidates may submit applications for more than one post. This post will have responsibility for inter- and transdisciplinary research programmes funding health research, for example through programmes such as Horizon Pillar 2 and EIC. The successful candidate will work in collaboration with RDO colleagues providing support for inter- and transdisciplinary research funding programmes. Post Status: Permanent Hours of Post: 35 hours per week Salary: Appointment will be made on the Administrative Officer 1 (1-3) €70,240 - €90,865 per annum) and in accordance with the Department of Finance guidelines. How to Apply: To assist the selection process, applicants should submit a Curriculum Vitae and a Cover Letter (maximum 1 x A4 page) that specifically addresses how their experience meets the requirements for this job. Please Note: Candidates who do not address the application requirements above in their cover letter will not be considered at the short list stage. Candidates should note that the interview process for this appointment will include the delivery of a presentation. Closing Date: 12 noon (Irish Standard Time) 16th October 2026 Application will only be accepted by applying online through the Trinity Jobs Portal must be made by the date and time specified. Any applications which are still in progress at the closing time on the specified closing date will be cancelled automatically by the system Late Applications will not be accepted. Interviews: It is intended that interviews will be held between 7th and 14th November, on the TCD campus. Skills: research or research administration national & International research funding landscap multi-sectoral engagement & facilitation IDR/ITD Horizon Pillar 2 and EIC health and healthcare research Benefits: pension

12 Months, Specific Purpose, Part-Time Post Position Summary We are currently recruiting a Research Support Officer - Clinical Nurse Manager 1 (Part-time) to support the PROSPER/Endo-Histo-Barrier -Omics team at Mercy University Hospital (MUH) and Cork University Hospital (CUH), with a dedicated office in CUH. It is an interdisciplinary project with multiple clinical research sites, laboratory projects and over several collaborators across the Republic of Ireland and the globe. In collaboration with the project manager and clinical fellows, the research nurse will manage study set-up, data collection/management, patient recruitment, adherence to all SOPs, and check accuracy of outcome measures. The research nurse will oversee the human studies recruitment and so will manage informed consent, discuss the study goals/sample collection with patients and prepare ethical study documentation for submission/approval, ensure appropriate follow up with patients and record any adverse events. They will collect basic demographic and clinical data, organise follow-up clinic visits, liaise with clinical research fellows regarding biomaterials collection, storage and transport, will implement GCP throughout. The follow-up visits will coincide with planned clinical visits and candidate will maintain close communication with their responsible clinician. UCC is an accredited research organisation and as such can form hosting agreements for the purpose of conducting research in the University. Project Title: Precision Endo-Omics: a quantitative approach to intestinal luminal imaging. Post Duration: 12 Months Salary: CNM1: €56,642 -€66,705 p.a. pro rata (0.7FTE) (As required by public pay policy for the higher education sector, new appointments to a direct entry recruitment grade will generally be at the minimum (1st point) of the relevant scale. For existing public servants, the restriction to the first point on scale may be varied where a person is appointed to the same or an analogous grade, role or position as their previous public service employment.) For an information package including further details of the post see Informal enquiries can be made in confidence to Professor Marietta Iacucci, Principal Investigator, Email: Applications must be submitted online via the University College Cork vacancy portal Queries relating to the online application process should be referred to quoting the job-title and project name. Candidates should apply, in confidence, before 12 noon (Irish Local Time) on Friday, October 24th, 2025. No late applications will be accepted. Please note that an appointment to posts advertised will be dependent on University approval, together with the terms of the employment control framework for the higher education sector. UCC is committed to creating and fully embracing an inclusive environment where diversity is celebrated. As a University we strive to create a workplace that reflects the diversity of our student population where people from a wide variety of backgrounds learn from one another, share ideas, and work collaboratively. UCC is committed to being an employer that recognises the value of diversity amongst its staff. We encourage applicants to consult our policies at and initiatives at and we welcome applications from everyone, including those who are underrepresented in the protected characteristics set out in our Equal Opportunities & Diversity Policy. UNIVERSITY COLLEGE CORK IS AN EQUAL OPPORTUNITIES EMPLOYER To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
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:**

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Research Scientist, Pharma**
At PPD, part of Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Location/Division Specific Information**
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
**Discover Impactful Work:**
The Research Scientist conducts and provides technical guidance on scientific method development and validation projects and/or other specialty technologies studies OR performs troubleshooting for own and others instruments, methods, procedures, and in writing protocols and reports. They design and execute method development/validation independently and interpret and review analytical data for self and others. They will routinely act as the technical project leader for multiple projects, provide updates, reviews and evaluates data, writes reports and protocols.
**A day in the life:**
+ Independently performs analytical method development/optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceuticals, specifically for techniques related to Physical and Chemical Characterization (for example HIAC, KF, FTIR, MFI, auto-titration)
+ Designs and executes experiments independently for self and others.
+ Reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
+ Writes, reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
+ Leads analytical (procedural and instrumental) troubleshooting sessions.
+ Assists business development group in technical sales and marketing
+ Leads in preparation and implementation of SOPs and quality systems, as well as developing innovative technology and in evaluating and implementing new capabilities.
+ Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
+ Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers
**Education and Experience**
+ Min. Degree or equivalent in Chemistry or similar
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
+ 8+ years experience that provides the knowledge and skills to perform the job
+ Significant industry experience within an analytical testing laboratory and GMP environment is essential
**Knowledge, Skills, Abilities**
+ Extensive technical expertise in equipment related to physical and chemical characterization of pharmaceutical products including but not limited to HIAC, KF, FTIR, MFI.
+ Ability to learn quickly and dedicate time to method/technical research into current techniques falling within physical testing team and new techniques that may be on-boarded in the future.
+ Proven experience of method development and validation
+ Ability to project management and deal with client audits
+ Ideally experience in leading CMC studies including method validation
+ Proven problem solving and troubleshooting abilities
+ Ability to independently perform root cause analysis for method investigations
+ Proven ability in technical writing skills
+ Time management and project management skills
+ Good written and oral communication skills
+ Ability to work in a collaborative work environment with a team
+ Ability to train junior staff
**Work Environment**
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
+ Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
+ Able to work upright and stationary and/or standing for typical working hours.
+ Able to lift and move objects up to 25 pounds.
+ Able to work in non-traditional work environments.
+ Able to use and learn standard office equipment and technology with proficiency.
+ May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
+ Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Accessibility/Disability Access**
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at *. Please include your contact information and specific details about your required accommodation to support you during the job application process.
+ This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

At Qualtrics, we create software the world's best brands use to deliver exceptional frontline experiences, build high-performing teams, and design products people love. But we are more than a platform-we are the creators and stewards of the Experience Management category serving over 18K clients globally. Building a category takes grit, determination, and a disdain for convention-but most of all it requires close-knit, high-functioning teams with an unwavering dedication to serving our customers.
When you join one of our teams, you'll be part of a nimble group that's empowered to set aggressive goals and move fast to achieve them. Strategic risks are encouraged and complex problems are solved together, by passing the microphone and iterating until the best solution comes to light. You won't have to look to find growth opportunities-ready or not, they'll find you. From retail to government to healthcare, we're on a mission to bring humanity, connection, and empathy back to business. Join over 5,000 people across the globe who think that's work worth doing.
**Senior Advisory Consultant, Strategy & Research Services**

**Why We Have This Role**
Our Strategy & Research (S&R) Services team is a small and high-performing group of implementation, advisory, and project management professionals. We work as a unified team to help our clients master and leverage Qualtrics software, tackling complex business challenges together. Our collective success is directly tied to our clients' success, and their advocacy for our work is our ultimate measure of impact. We're looking for a proactive and commercially-minded market research consultant to join our team. We're not looking for someone to simply manage projects; we want a strategic partner for our clients and a key decision-maker on their programmes. You'll use your deep quantitative research expertise to design, deliver, and evolve research initiatives, ensuring they drive meaningful business outcomes. You'll need to be an independent contributor who thrives in ambiguity and provides clear guidance to both clients and internal teams.
**What You'll Do**
Your primary function is to serve as a trusted advisor to our clients and internal teams. You will:
+ Proactively identify and capitalise on new research opportunities, transforming client challenges into strategic solutions that drive tangible business growth and unlock new revenue streams.
+ Partner with our client management teams to ensure clients are extracting maximum value from their research programmes. This includes leading data interpretation sessions, creating concise thought pieces, and recommending new research approaches.
+ Serve as a key strategic partner in pre-sales discussions, leveraging your expertise to design bespoke research methodologies that win new business and set our clients up for long-term success.
+ Play a key advisory role during the full lifecycle of a client engagement, from initial programme design to delivering compelling insights. This includes conducting in-depth data analysis, producing professional reports, and providing insightful recommendations that enable clients to take clear action
+ Act as a change agent, guiding clients through the transition from traditional to tech-led research by confidently leading complex conversations and demonstrating the value of our innovative approach.
+ Mentor and train junior team members, setting a high bar for excellence and embodying the positive culture of our team.
+ Function as a key decision-maker on programme strategy and design, owning the execution and delivery.
**How You'll Find Success**
Success in this role is not just about delivering a project; it's about building a client relationship that convinces them of the program's value and future potential. You will find success by:
+ Demonstrating strategic thinking in all aspects of your work.
+ Thriving in an environment of ambiguity, where you are empowered to make decisions and create solutions.
+ Consistently delivering flawless results and earning your place as a trusted advisor to clients.
+ Embodying a continuous improvement and growth mindset, always seeking new and more effective ways to deliver impact.
**How You'll Grow**
+ Shape the future of our division by influencing products, processes, and deliverables.
+ Evolve into a strategic thought leader and develop unparalleled expertise within Qualtrics.
+ Mentor and train junior team members, setting a precedent for leadership and excellence.
+ Gain exposure to diverse projects and strategic initiatives that have a tremendous departmental and organizational impact.
+ Build your research expertise across different methodologies (e.g., Brand, UX, Campaign Evaluations, Pricing Studies, Concept Tests, etc.).
**What We're Looking For On Your CV**
+ A bachelor's or advanced degree in a relevant field (e.g., business, social sciences, statistics).
+ A minimum of 8 years of experience in a custom research, market research, or business analytics role, with a strong emphasis on client-facing advisory.
+ A proven track record of proactive contributions and strategic problem-solving.
+ Exceptional presentation skills, with a strong ability to translate complex data into clear, compelling narratives.
+ Experience with Qualtrics or similar research platforms is highly preferred, but not a requirement.
+ A natural ability to thrive as an independent contributor in a fast-paced, unstructured, and highly collaborative environment.
+ The flexibility to evolve in the role as needed to align with company evolution, acknowledging that we are a tech company and must always be agile.
+ Excellent written and verbal communication skills.
**What You Should Know About This Team**
+ We are a small, high-performing, and highly profitable team with a focus on strong delivery and commercial acumen.
+ Our client satisfaction rate is incredibly high, and identifying ways to continue to delight stakeholders is key to our mission.
+ We are agile and lean in across functions when and if needed-every team member is a key contributor to our collective success.
+ The day-to-day in this role is dynamic and fast-paced; the ability to prioritize and stay focused is critical to success.
**Our Team's Favourite Perks and Benefits**
+ Qualtrics Experience Program - A bonus each year for an experience of your choosing.
+ Worldwide and diverse community that enjoys helping each other.
+ We take pride in creating an open and collaborative work space.
+ At Qualtrics we are constantly working to create an environment where everyone feels safe and comfortable coming to work and can, as a result of our culture, make their best possible contribution to our team.
+ Check out more about our benefits here ( Qualtrics Hybrid Work Model:** Our hybrid work model is elegantly simple: we all gather in the office three days a week; Mondays and Thursdays, plus one day selected by your organizational leader. These purposeful in-person days in thoughtfully designed offices help us do our best work and harness the power of collaboration and innovation. For the rest of the week, work where you want, owning the integration of work and life.
_Qualtrics is an equal opportunity employer meaning that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other protected characteristic._
_Applicants in the United States of America have rights under Federal Employment Laws: Family & Medical Leave Act ( , Equal Opportunity Employment ( , Employee Polygraph Protection Act ( is committed to the inclusion of all qualified individuals. As part of this commitment, Qualtrics will ensure that persons with disabilities are provided with reasonable accommodations. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your Qualtrics contact/recruiter know._
_Not finding a role that's the right fit for now? Qualtrics Insiders is the one-stop shop for all things Qualtrics Life. Sign up for exclusive access to content created with you in mind and get the scoop on what we have going on at Qualtrics - upcoming events, behind the scenes stories from the team, interview tips, hot jobs, and more. No spam - we promise! You'll hear from us two times a month max with fresh, totally tailored info - so be sure to stay connected as you explore your best role and company fit._

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
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:**