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Search Results for Clinical Project Manager
Job Title. | Location | Salary | Actions |
Associate Director Clinical Trial CapabilitiesAssociate Director Clinical Trial Capabilities Our client, a global pharmaceutical organisation are currently recruiting an Associate Director to join their Clinical Trials Capabilities team on a permanent basis. As Associate Director you will lead the clinical trial capabilities in support of clinical development. This is an exciting opportunity which will allow you to provide leadership, direction and technical support to the Clinical Trial Capabilities Teams focusing on results and driving efficiency to achieve goals and objectives Responsibilities: Lead and co...Location: Cork, |
Cork | Not Disclosed | |
Neurovascular Research ManagerJob title: Neurovascular Disease Research Engineer Location: Ballybrit, Galway Benefits: Hybrid working model, competitive salary, 13% yearly bonus, pension and Healthcare. Company: My client is an emerging leader in Neurovascular care in the Medical Device industry. Located in a European hub for the Medical Device industry my client works closely with physicians from around the world to develop devices used in the endovascular treatment of strokes. Role: The NVD Research Manager will be part of the Neuro Thromboembolic Initiative (NTI%2...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Head of Clinical ResearchHead of Clinical Research Our Sligo based client are currently looking for a Head of Clinical Research to join their team on a permanent basis. As Head of Clinical Research, you will be responsible for overseeing all clinical studies related to products developed. You will be responsible for ensuring the planning, implementation and management of clinical trials and other related activities by designing and executing studies to support regulatory submissions and post-market surveillance Responsibilities Develop and execute clinical research strategies, plans, and budge...Location: Sligo, |
Sligo | Not Disclosed | |
Clinical Program ManagerClinical Program Manager Our Dublin based client are currently recruiting for a Clinical Program Manager to join their team on a permanent basis. As Clinical Program Manger, you will be responsible for the planning, development and management of Clinical Operations activities. Responsibilities Oversee clinical project and site management activities including trial timelines, budgets, resources and vendors Leads the development of clinical trial protocols; participates in the development of the overall clinical plan, drafts protocols, collaborates on statistical an...Location: Dublin, |
Dublin | Not Disclosed | |
Senior Manager Clinical Trial Cost ForecastingSenior Manager Clinical Trial Cost Forecasting Our client, a global pharma organisation, are currently recruiting for a Senior Manager Clinical Trial Cost Forecasting to join the global centre of excellence for clinical trials on a permanent basis. As Senior Manager Clinical Trial Cost Forecasting, you will lead the Budgets and Costing team with an overall goal to support Investigator Grants Budget Development and Clinical Costing and Forecasting. This is a hybrid working role. Responsibilities: Enable the flexibility of resources from the team, par...Location: Cork, |
Cork | Not Disclosed | |
Clinical Trial Design Site Training AssociateClinical Trial Design Site Training Associate Our client, a global pharma organisation, are currently recruiting for a Clinical Trial Design Site Training Associateto join their global centre of excellence for clinical trials on a permanent basis. The ideal candidate will be experienced in clinical development and clinical trials cost forecasting. This is a hybrid working role. As ClinicalTrial Design Site Training Associate, you will provide technical, project and operational expertise to support the strategy for a variety of aspects within the clinical programs which ...Location: Cork, |
Cork | Not Disclosed | |
Associate Director Clinical Trial Design Clinical CostingAssociate Director Clinical Trial Design Clinical Costing Our client, a global pharma organisation, are currently recruiting for an Associate Director of Clinical Trial Design Clinical Costing to join their global centre of excellence on a permanent basis. The ideal candidate will be experienced in clinical development and clinical trials cost forecasting. This is a hybrid working role. Responsibilities: Develop strong working relationships with collaborators (i.e., CDDA functional leadership, Design Hub, Clinical Laboratory Sciences, Procurement, Clinical Devel...Location: Cork, |
Cork | Not Disclosed | |
GCP InspectorGCP Inspector Reporting to the GCP/Pharmacovigilance Inspection Manager, the role of the GCP Inspector is to evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation (in Ireland), European Community Directives, Regulations and Guidance. These sites may include: ·Sites where clinical trials are conducted ·Sites responsible for management, administration or data collection activities for clinical trials, (sponsor organisations, clinical research organisations) ·Clinical t...Location: Dublin, |
Dublin | Not Disclosed | |
Director, Clinical Development (Oncology)Our client is a Global Biopharma who has been a leading innovator in the field of virology, having developed many of today’s leading medicines for treating and preventing HIV and viral hepatitis. More recently, they have expanded its oncology portfolio, and seeks to become a leader in this critical disease area. In this role as Director, Clinical Development, you will lead regional components of clinical trial programs in Oncology clinical development. For the assigned projects, you are accountable for various aspects of regional ongoing clinical trial program-relate...Location: South East, |
South East | Not Disclosed |
Clinical Project Manager Career Profile
Clinical Project Manager
The clinical project manager, in conjunction with leading local and global investigators, functions to ensure effective and efficient management and support of clinical research studies from an administrative perspective, in accordance with ICH-GCP, Research Governance Framework and IMB regulations.
The Clinical Project Manager will have a leading role in planning, coordinating and completing specialised clinical research projects. They will need excellent communication, presentation skills and the ability to organise both themselves and others. They will be responsible for the day-to-day management of clinical research studies and will work closely with the Principal Investigators to ensure their successful completion.
Key Responsibilities
- Communicate effectively with health care professionals, researchers, administrative staff and users of the health service both nationally and internationally.
- Motivate and maintain a collaborative group, including groups across multiple jurisdictions (UK and Ireland).
- Produce regular reports and progress reports appropriate for collaborators, Steering Groups and Monitoring and Ethics Committees as appropriate.
- Plan contact with collaborators whether that be with individuals, groups or the whole group and monitor effectiveness of that contact.
- Liaise with national and international Ethics Committees as required.
- Liaise with funding bodies, the host institution and any other relevant institutions.
- Ensure all trial procedures are developed according to the relevant Good Clinical Practice and Data Protection Guidelines.
- Monitor, in conjunction with the relevant PIs, adverse events and ensure appropriate action.
- Where appropriate, assist with publishing in relevant scientific journals throughout duration of study.
- Employ standard project management techniques to achieve the project goals and objectives in a timely fashion
- Monitor budget and report back to allow efficient and accurate budget management
- Recruit, train, appraise and supervise members of trial team and work with them to ensure successful completion of the project.
- In conjunction with the PIs, design, produce and regularly update all trial materials.
- Carry out projects with a view to establishing a library of general SOPs required for clinical research.
- Contribute to the management and effectiveness of the Institute as a member of its Management Team.
- Network with other Clinical Research Networks in Dublin and across Ireland.
Qualifications & Experience
- Minimum of 4-5 years experience of coordinating and/or managing clinical trials or similar health related projects (e.g. CRA, CPM)
- Degree or Masters level qualification in a relevant scientific/healthcare field
- Knowledge of PRINCE 2 or similar Project Management Methodology
- Knowledge of MS Project or similar software tools for project planning and monitoring
- Knowledge of relational databases and data management an advantage
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Clinical Research | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: info@clinicalresearch.ie
Copyright © 2012 Life Science Recruitment Ltd
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Clinical Research | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: info@clinicalresearch.ie
Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. More information on our cookie policy can be found in our Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 |
Web Design / SEO by WebScience | Valid XHTML - CSS







