What Veterinary Clinics Jobs are in Ireland?

Clinical Nurse Manager 1 Permanent Contract - 22.5 hours per week Based in CRC Children's Disability Network Teams, Waterford The CRC Children's Disability Network Teams (CDNT) will be providing intervention to children from the age of 0-18 years, presenting with complex developmental needs requiring inter-disciplinary intervention. Our services are based upon a Family Centered Practice Model in line with the Progressing Disability Services. This is an exciting opportunity to work as part of a dynamic team in Waterford. The successful candidate will have the following essential requirements: Be a registered RNID, RCN or RGN on the Register of Nurses kept by the Nursing and Midwifery Board of Ireland (NMBI) and maintain a live a live PIN. Have a minimum of 3 years post qualification experience to include at least 1 year in a community setting. Possess the requisite knowledge and ability, (including a high standard of clinical and administrative capacity), for the proper discharge of the duties of the office. Clinical experience to include N/G, PEG feeding, respiratory support such as CPAP BiPAP, tracheostomy, catheterisation and continence care. Full driver's license and access to car. Desirable requirements: Experience working with children with Autism Spectrum Disorder Experience working with children with physical disabilities Experience working with children with intellectual disabilities Experience completing Assessment of Need It must be clearly demonstrated in your CV and supporting statement how you meet the required skills, competencies and knowledge for the post. Department of Health Salary Scale apply, CNM1 (€57,780 - €68,046 Annual Salary). (Salary will be pro-rated for 0.6WTE, i.e €34,668 - €40,827). Please apply by clicking on the 'Apply Now' button below. Applications must be received on or before 23rd July 2026. Informal enquires to Grainne DePaor CDNM Waterford on . A panel may be created from this campaign from which current and future permanent, specified purpose, whole-time and part-time posts for CRC Children's Disability Services will be filled. Data Protection: Please refer to to learn more about how we handle your personal data and the rights that you have during the recruitment cycle. This role is subject to HSE Approval We reserve the right to close this competition early if we receive a very high volume of applications. #CR Benefits Paid Time-Off for Vacation and Sick Days Professional Development + Growth EAP (Employee Assistance Programme) Opportunities for Advancement Work/Life Balance Pension Scheme Competitive salary Learning and development opportunities Maternity Leave & Pay Paternity Leave & Pay 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.

JR Principal Clinical Data Science Lead
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Principal Clinical Data Science Lead at ICON, you will be responsible for guiding and oversee the application of advanced data science methodologies to clinical research and development.
**What You Will Do:**
Your focus will be on coordinating clinical data science delivery, resolving issues, and developing team capability.
Key responsibilities include:
+ Leading the design and implementation of advanced data science methodologies and statistical models to support clinical research and data analysis.
+ Guiding a team of data scientists and analysts in the development and execution of data-driven strategies to optimize clinical trial design and outcomes.
+ Collaborating with cross-functional teams, including clinical, biostatistical, and regulatory experts, to ensure integration of data science insights into clinical development programs.
+ Driving innovation in the use of data science tools and techniques, including machine learning and predictive analytics, to enhance the efficiency and effectiveness of clinical trials.
+ Providing strategic direction and oversight for data management and analysis processes, ensuring compliance with regulatory requirements and industry best practices.
+ Communicating complex data findings and insights to stakeholders, including senior leadership and external partners, to support decision-making and strategic planning.
**Your Profile:**
You will have solid clinical data science experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
+ Bachelor's degree in life sciences, computer science, or a related discipline
+ Extensive experience in clinical data science, with a strong track record of applying data science methodologies to clinical research and development.
+ Proven leadership skills, with experience managing teams of data scientists and guiding data science initiatives in a clinical or biopharmaceutical setting.
+ Expertise in data analysis, statistical modeling, and machine learning techniques, with proficiency in relevant software and programming languages.
+ Excellent communication and collaboration skills, with the ability to convey complex data insights to both technical and non-technical stakeholders.
+ Strong understanding of clinical trial processes, regulatory requirements, and best practices in data management and analysis
\#LI-SA1
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

Role Title:Clinical Nurse Manager II: Clinical Research Nurse in Cancer Job Reference Number: Closing Date:Sunday ,26th July 2026 Purpose of the Role: The post holder will be responsible for the co-ordination of a defined group of clinical trials from set up to archiving and meeting agreed patient recruitment targets. The role of the CNM II is to: Ensure that all research undertaken within the hospital safeguards the wellbeing of the patients. Ensure that research is conducted within requirements of a multi-regulated clinical research environment. Facilitate the production of high-quality research. Raise the profile of the clinical research nurse and clinical trials. Ensure delivery of divisional, Trust and national objectives. Provide leadership & management of a specific research team. Clinical Research Co-ordination Work autonomously in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical research protocols. Undertake feasibility and risk assessments of clinical trial protocols in conjunction with Lead Research Nurse, Principal Investigator and Study Start Up team. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific and national targets. Initiate new recruitment strategies for recruiting patients to clinical trials. Lead on the delegation of all trial related activities to research team members (clinical and administrative) and ensure compliance with protocols, SOPs and ICH/GCP. Arrange and facilitate clinical trial related meetings. Clinical Service and Professional Responsibilities Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and careers regarding prognosis Responsible for the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel. Demonstration of expert knowledge in specialist area to maintain clinical excellence. Support Lead Research Nurse (CNM III) in delivering Cancer Clinical Trials Unit strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals. Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training (e.g., GCP) in accordance with local policy Ensuring care delivery standards in accordance with trial protocol, local policy, NMBI Code of Practice Conduct and current best practice Development and maintenance of a high-quality service by: Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial. Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention. Contribute to development of specialist Standard Operating Procedures and guidelines Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients. Participate in monitoring and audit activities within research team Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning. Promote the role of the clinical research nurse as an integral part of the healthcare system. Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development. Participation in hospital-wide education programs and study days. Obtain clinical supervision as appropriate. To keep up to date with Hospital, Irish and EU developments for the management of clinical research ensuring timely, effective implementation of changes. Staff Management and Development In conjunction with the CNM III, provide the induction, continued supervision and management of the research teams. In conjunction with the CNM III, be responsible for ensuring all members of the research nurse team undergo regular appraisal and support appropriate training and development opportunities in line with role requirements. Provide specialist education and training in relation to clinical trials to all key stakeholders. Disseminate information by attendance and /or presentations at local, national and international conferences/meetings Be responsible for the development of members of the research team. Quality, Patient Safety & Risk Management Proactively identify, document, assess and manage risks in line with the Hospitals risk management framework. Ensure risks and controls within each area of accountability are clearly articulated, with assigned owners, realistic mitigation actions, timelines and monitoring arrangements. Maintain appropriate oversight of risks, ensuring they are routinely reviewed. Utilise regular audit and evaluation for the purpose of assurance and identifying required areas for improvement. Strengthen quality, safety and risk practices across areas of accountability. Drive a culture of safety, accountability, quality assurance, systems learning and continuous improvement. Support and adhere to all relevant regulatory and governance standards. Support the implementation of quality improvements within the hospital as directed by the Hospital Board and Executive Management Group in response to quality, safety and risk management. * The above Role Profile is not intended to be a comprehensive list of all duties involved and consequently the post holder may be required to perform other duties as appropriate to the post which may be assigned to them from time to time and to contribute to the development of the post while in office. This Role Profile will be subject to review in the light of changing circumstances. Required: Registered General Nurse with The Nursing Midwifery Board of Ireland (NMBI), or eligible to register. 5 years post-registration experience in an acute hospital setting or relevant clinical area within the last 7 years. A minimum of 1 years experience in clinical trial co-ordination as part of a research team. At least 1 year experience at CNM I level showing organisational and management skills. Completed Good Clinical Practice Course (ICH GCP E6R3). Highly effective communication skills. Experience in co-ordinating care pathways for patients participating in clinical trials. Demonstrate understanding and active participation in the conduct of clinical trial delivery. Experience of working autonomously and part of multidisciplinary team. Demonstrate I.T. skills including the use of data bases and excellent keyboard skills. Desired: Postgraduate qualification in Oncology/Haematology nursing or a willingness to complete when in post. Management course. Working knowledge of healthcare patient record systems and sponsor data systems

Clinical Data Standards Consultant - ADaM ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. Job Advert Posting A Clinical Data Standards Consultant is responsible for supporting the operational staff in the use of ADaM and the capture for statistical analysis within the Medidata standard. They will develop tools to increase the efficiency, timeliness and quality of deliverables for data collection, tabulation, analysis and reporting. They will also define and collect metrics about the use of standards. They will participate in the development of training of the operational staff in the areas of their expertise. What You Will Do: Serve on Sponsor Standards and Technology Leadership teams. Consult with clients on sponsor-specific CDISC centric implementation projects. Participate in industry groups focused on the development of standards related initiatives (e.g. CDISC, PhUSE etc.). Author, maintain, implement, and report status for Standards Related Project Plans. Responsible for the implementation, strategy, and configuration of a metadata repository used to manage libraries of CDISC related metadata, terminology and related standards. Mentor Clinical Data Standards Consultants. * Lead Subject Matter Expert teams on topics relevant to standards. Identify areas for process improvement which may increase productivity, quality and / or compliance of deliverables in the areas from data collections through analysis and reporting. Participate in the analysis of metrics and in creating recommendations to the management teams on process improvements together with the Director of Global Data Standards. Your Profile: Minimum of 5 years of experience in industry in a role demonstrating knowledge of clinical data standards used by biometrics. An undergraduate degree or international equivalent from an accredited institution Demonstrated expertise in CDASH, SDTM standards and associated controlled terminology with a good understanding of CRF design concepts. Excellent communication skills with demonstrated leadership ability. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply To be considered for this role you will be redirected to our careers page & prompted to create a jobseeker account here. To start the process, click the Continue to Application or Login/Register button below. Benefits: Work From Home

Excellent Base Salary + Bonus + Company Car + Pension + Health Insurance + Lunch Allowance Territory: Republic of Ireland (candidate ideally based in Leinster) 12-Month Contract Are you a relationship-driven sales professional who enjoys building trusted partnerships, delivering training, and supporting healthcare professionals in improving patient outcomes? We're partnering with a highly regarded global healthcare organisation to recruit a Territory Manager for the Republic of Ireland. This is an excellent opportunity to join a business known for its outstanding culture, supportive leadership team, and long-standing employee retention. This is not a transactional sales role. Success is built through developing strong relationships with nursing teams and healthcare professionals, providing education and support, and becoming a trusted partner to your customers. Why Join? Join a market-leading healthcare organisation with an excellent reputation Strong focus on relationship building rather than hard selling Opportunity to work closely with nursing teams across Ireland Significant emphasis on training, education, and customer support Family-oriented culture with a genuine sense of togetherness Supportive and collaborative management team Strong employee retention and long-term career opportunities Autonomy to manage your territory with excellent backing and resources The Role Covering the Republic of Ireland, you will be responsible for managing and developing existing customer relationships while identifying opportunities for growth within your territory. Working closely with nursing teams and other healthcare professionals, you will provide product education, deliver training, and support customers in their day-to-day clinical practice. By building trusted partnerships, you will help drive business growth while ensuring customers receive exceptional support and service. Key Responsibilities Build and maintain strong relationships with nurses and healthcare professionals throughout the territory Deliver product training, education, and ongoing customer support Develop and grow existing accounts while identifying new business opportunities Execute territory business plans and achieve agreed sales objectives Maintain a strong pipeline of opportunities across the territory Conduct regular customer visits and account reviews Drive customer engagement and satisfaction initiatives Become a trusted clinical and commercial partner to your customer base Maintain accurate CRM records and activity reporting Monitor market trends and competitor activity Collaborate with colleagues to maximise territory performance and customer outcomes About You 2-5 years' experience within healthcare, medical device, pharmaceutical, clinical products, patient care, wound care, healthcare consumables, or a related sales environment Proven ability to build strong, long-term customer relationships Experience working with nurses or healthcare professionals would be highly advantageous Comfortable delivering training, education, and presentations Strong communication and stakeholder management skills Commercially focused with a customer-first approach Self-motivated and capable of managing a territory independently Well organised with strong planning and prioritisation skills Team-oriented with a collaborative working style Full clean driving licence Package Strong Base Salary Performance Bonus Company Car Private Health Insurance Pension Lunch Allowance Comprehensive Training & Development Supportive Team Environment Excellent Company Culture If you're looking for a role where relationships, training, customer support, and culture are valued just as highly as sales performance, we'd love to hear from you. Adecco Ireland is acting as an Employment Agency in relation to this vacancy. Skills: medical territory sales Benefits: pension healthcare company car

JR Senior Clinical Data Science Lead ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Senior Clinical Data Science Lead at ICON, you will lead the analysis, interpretation, and management of clinical data to drive the success of our clinical trials. What You Will Do: You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations while acting as the functional lead across multiple low to moderately complex studies. Key responsibilities include: Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, data review, and reporting. Leading multiple low/moderately complex studies as the functional Clinical Data Science Lead and acting as a resource for colleagues with less experience. Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs. Overseeing the analysis and review of clinical data to provide actionable insights that inform study decisions and outcomes. Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements. Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research. Applying project management skills to proactively manage timelines, resource requirements, and financial tracking. Developing a detailed understanding of protocol content and interpreting critical data and data review requirements. Reacting and adapting requirements, processes, and timelines in an agile manner to meet project and business needs. Tracking study progress and keeping functional management and project management informed of issues that may affect project target dates, scope, or budget, escalating risks in a timely manner. Working independently and with other project leads, as needed, to negotiate timelines and key deliverables with clients, external customers, and internal departments. Understanding project-level revenue recognition and forecasting processes, providing input on actual and forecasted units/hours (revenue and resources) to the Clinical Data Science Project Manager. Undertaking other responsibilities as assigned. Your Profile: You will have solid clinical data science experience, with the ability to manage competing priorities, lead multiple studies, solve complex problems, and support the development of your team. Required qualifications and experience: Bachelor's degree in life sciences, computer science, or a related discipline. Typically 5-8 years of experience in Clinical Data Science, Clinical Data Management, or a related field. An equivalent combination of education, training, and relevant experience may be considered in place of the stated education and experience. Extensive experience in clinical data science, with a strong focus on clinical data management, data review, and analysis in clinical trials. Enhanced knowledge of clinical data management, clinical data science, and clinical data review activities. Applied project management skills, including experience managing timelines, resource requirements, and financial tracking. Detailed understanding of protocol content and interpretation of critical data and data review requirements. Strong leadership skills and a proven ability to lead multiple studies, manage cross-functional teams, and act as a resource for colleagues with less experience in a fast-paced, matrix environment. Strong problem-solving skills with the ability to analyse and investigate complex issues, identify solutions that are not readily apparent, and anticipate future challenges. Ability to work independently, establish approaches, and lead resources to achieve operational and strategic objectives with impact on medium-term goals. Expertise in data analysis tools, statistical software, and data visualization techniques. Excellent communication, interpersonal, and stakeholder management skills, with the ability to adapt communication style, influence stakeholders, present and defend complex analyses, and secure approval on complex matters #LI-SA1 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply To be considered for this role you will be redirected to our careers page & prompted to create a jobseeker account here. To start the process, click the Continue to Application or Login/Register button below. Benefits: Work From Home

JR Principal Clinical Data Science Lead ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Principal Clinical Data Science Lead at ICON, you will be responsible for guiding and oversee the application of advanced data science methodologies to clinical research and development. What You Will Do: Your focus will be on coordinating clinical data science delivery, resolving issues, and developing team capability. Key responsibilities include: Leading the design and implementation of advanced data science methodologies and statistical models to support clinical research and data analysis. Guiding a team of data scientists and analysts in the development and execution of data-driven strategies to optimize clinical trial design and outcomes. Collaborating with cross-functional teams, including clinical, biostatistical, and regulatory experts, to ensure integration of data science insights into clinical development programs. Driving innovation in the use of data science tools and techniques, including machine learning and predictive analytics, to enhance the efficiency and effectiveness of clinical trials. Providing strategic direction and oversight for data management and analysis processes, ensuring compliance with regulatory requirements and industry best practices. Communicating complex data findings and insights to stakeholders, including senior leadership and external partners, to support decision-making and strategic planning. Your Profile: You will have solid clinical data science experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience: Bachelor's degree in life sciences, computer science, or a related discipline Extensive experience in clinical data science, with a strong track record of applying data science methodologies to clinical research and development. Proven leadership skills, with experience managing teams of data scientists and guiding data science initiatives in a clinical or biopharmaceutical setting. Expertise in data analysis, statistical modeling, and machine learning techniques, with proficiency in relevant software and programming languages. Excellent communication and collaboration skills, with the ability to convey complex data insights to both technical and non-technical stakeholders. Strong understanding of clinical trial processes, regulatory requirements, and best practices in data management and analysis #LI-SA1 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply To be considered for this role you will be redirected to our careers page & prompted to create a jobseeker account here. To start the process, click the Continue to Application or Login/Register button below. Benefits: Work From Home

**About the Role**
We are seeking a **Clinical Specialist** to support our Coronary portfolio, focusing on **OCT Imaging, PressureWire (Physiology), and Orbital Atherectomy (Calcium Management Therapies)** .
In this role, you will partner closely with interventional cardiologists, cath lab teams, and internal stakeholders to deliver **best-in-class clinical training, procedural support, and therapy adoption** across NHS and private hospitals.
You will play a critical role in executing the **Complex PCI (PCIO) and Orbital Atherectomy (OAS)** strategy within your region while contributing to broader Coronary business objectives.
**Key Responsibilities**
+ Provide **in-lab case support** across OCT, physiology, and calcium management therapies
+ Deliver **hands-on technical support** to physicians and nursing staff during procedures
+ Lead **clinical education and product training sessions** for healthcare professionals
+ Support **therapy adoption and growth** , identifying opportunities through account and market analysis
+ Build strong relationships with **Key Opinion Leaders (KOLs)** and hospital stakeholders
+ Collaborate with Territory Managers and Regional Sales Manager on **account strategy and procedural coverage**
+ Support **product launches and implementation plans** , ensuring effective customer engagement
+ Participate in **local and international congresses, meetings, and training events**
+ Maintain accurate records and complete administrative requirements (e.g., CRM updates, forecasts, expenses)
+ Ensure compliance with all **clinical, regulatory, and company standards**
**What You'll Bring**
+ Bachelor's degree (preferably in a scientific or healthcare-related field)
+ Experience in a **Cath Lab, clinical specialist role, or relevant healthcare setting**
+ Strong understanding of **interventional cardiology procedures and hospital environments**
+ Knowledge of **vascular anatomy and physiology (preferred)**
+ Excellent **communication and presentation skills**
+ Ability to build strong, professional relationships in dynamic clinical settings
+ High level of professionalism, ethics, and collaboration
+ Strong organisational and IT skills (MS Office tools)
+ Willingness to travel **up to 70%** across your region
**What You'll Gain**
+ Exposure to **cutting-edge coronary technologies** (OCT, PressureWire, Orbital Atherectomy)
+ Opportunity to work closely with leading clinicians in **Complex PCI**
+ A highly collaborative environment with strong clinical and commercial alignment
+ Ongoing development through **training, coaching, and international collaboration**
**What We Offer**
Attractive compensation package that includes **competitive pay and structure Bonus** , as well as benefits such as
+ Private Health Insurance for you and your family
+ Occupational Pension Scheme with an excellence contribution rate
+ Bonus Target
+ Life assurance
+ Career Development
+ Growing business plus access to many more benefits
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.**
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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