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Search Results for Clinical Project Manager
Job Title. Location Salary Actions

Director, Quality & Compliance (GCP)

Our client is a global Biopharma organisation who play a crucial role in developing life-saving therapies. They are seeking a Clinical Quality and Compliance Director who is ready to dive-in to support our clients clinical development programs. As a Clinical Quality and Compliance Director, you will support and work with our clinical study management teams and teammates across R&D Quality and Compliance. They need someone with strong leadership skills, expert Good Clinical Practice (GCP) knowledge, audit skills, communication, facilitation skills, and the ability to...

Location: Dublin,
Director, Quality & Compliance (GCP)
Dublin Not Disclosed

Director of Clinical Pharmacology (Infectious Diseases)

Our client is a leading Bio-Pharma who are establishing a new office in Dublin in the area of Clinical Research. As a Director within the Clinical Pharmacology Group, the successful person will have ultimate responsibility and accountability for clinical pharmacology programs in the area of HIV and emerging viral infections. As a member of the Clinical Pharmacology team this person shall have unparalleled opportunity to be involved with every aspect of the product development process, from first-in human through approval, including post-marketing activities. In this role, ...

Location: Dublin,
Director of Clinical Pharmacology (Infectious Diseases)
Dublin Not Disclosed
Other Clinical Research Jobs
Job Title Location Salary Actions
Senior Project Manager - Tech transfer Dublin 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