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Snr QA Officer
Dublin North
API Purchaser
Dublin
Biostatistician
Dublin City Centre
QA Manager
Dublin North
Product Specialist (Microbiology)
Republic of Ireland
QA Manager
Meath
Senior CRA
Dublin
R&D Engineer
Galway
Program Manager
Westmeath
Buyer
Cork
Head of Quality
Dublin West
QA Manager
Dublin West
R&D Engineer
Dublin
Snr QA Specialist
Dublin South
QA Manager Biologics
Dublin West
Consultant
Brian Christensen
Life Science

+353 (0)1 685 47 47
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Search Results for Clinical Project Manager
Job Title. Location Salary Actions

Clinical Development Associate

**This role is exclusively with Life Science Recruitment** Our client is a start-up medical device organisation based in north Dublin. This hiring manager for this role is very highly-regarded in the industry and the successful individual can expect to learn a lot about medicla device clinical development and clinical programme management in a short space of time. Purpose of the role: To support the execution of our client's clinical development plan by delivering first in class projects. Job Responsibilities: This role will provide scientific and technical support to the ...

Location: Dublin,
Clinical Development Associate
Dublin Not Disclosed
Other Clinical Research Jobs
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Development Leader Dublin Not Disclosed
Projects Leader Dublin Not Disclosed
Research and Development Compliance Specialist Galway Not Disclosed
Senior CRA Dublin Not Disclosed
Senior CRA Dublin Not Disclosed
Senior CRA Dublin Not Disclosed
Biostatistician Dublin City Centre 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