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Search Results for Clinical Project Manager
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Senior Clinical Project Manager Our Dublin based client are currently recruiting for a Senior Clinical Project Manager to join their team on a permanent basis. As Senior Clinical Project Manager you will be responsible for maintaining knowledge and ensuring compliance with ICH-GCP, regulatory requirements, applicable guidelines, SOPs (Standard Operating Procedures), study protocols and project-specific procedures, manage assigned studies in line with SOPs and manage successful execution of one or multiple projects. The role reports directly into the Head of Operations and Cl...

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Location: Republic of Ireland,
Clinical Research Associate (CRA) 		Republic of Ireland Not Disclosed

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Our client is a Global Biopharma who are establishing a Paediatric Centre of Excellence in Dublin that will be responsible for the management and execution of Paediatric Clinical Trials, across all therapeutic areas, around the world. The Clinical Operations team in Dublin is a pivotal function within this Centre of Excellence. In partnership with Clinical Research, Medical Affairs and other Development Operations functions, Clinical Operations ensures that all clinical trial activities are performed in accordance with applicable SOPs, company policies and regulatory gui...

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Contract & Budgets Trial Capabilities Associate Fluent German 		Cork Not Disclosed

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Clinical Trial Start Up Associate- Fluent Romanian Our client, a global pharmaceutical organisation are currently recruiting for a Fluent Romanian speaking Clinical Trials Start Up Associate to join their team on a permanent basis. As Clinical Trial Start Up Associate you will be responsible for ensuring the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout, obtaining clinical trial authorizations and ethical approvals,execution of the budget and contract, and activiti...

Location: Cork,
Clinical Trial Start Up Associate Fluent Romanian 		Cork Not Disclosed

Clinical Trials Project Manager

Clinical Trials Project Manager Our client, a global pharmaceutical organisation based in Cork are currently recruiting for a Clinical Trials Project Manager to join their newly created team on a permanent basis. As Clinical Trial Project Manager you will lead the cross-functional study team in the development and execution of clinical trials and will be responsible both regionally and globally to deliver trials with quality, on time, and within scope and budget. Responsibilities Use project management skills, processes and tools to develop and execute loca...

Location: Cork, Republic of Ireland,
Clinical Trials Project Manager 		Cork Not Disclosed

Clinical Trial Associate German Speaking (based in Ireland)

Clinical Trial Associate German Speaking (based in Ireland) Our Cork based client are currently recruiting for an experienced fluent German speaking Clinical Trial Associate to join their team on a permanent basis. The Clinical Trial Capabilities Team provides clinical trial capabilities in support of clinical development. As Clinical Trials Associate you will be accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout. You will be responsible for obtaining clini...

Location: Cork,
Clinical Trial Associate German Speaking (based in Ireland) 		Cork Not Disclosed

Clinical Trial Associate German Speaking (based in Ireland)

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Clinical Trial Associate German Speaking (based in Ireland) 		Cork Not Disclosed
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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