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

Associate Director Clinical Trials Project Manager

Associate Director Clinical Trials Project Manager Our client, a global pharma company, are currently recruiting for an Associate Director Clinical Trials Project Manager to join their team on a permanent basis. As Associate Director you will lead the creation and execution of the exploratory and biopharmaceutics clinical development and delivery plan, with technical leadership and delivery oversight of clinical research trials within the development plan. Responsibilities Plan and deliver exploratory and biopharmaceutical clinical molecules and submit...

Location: Cork,
Associate Director Clinical Trials Project Manager 		Cork Not Disclosed

Associate Director - Clinical Trials Project Manager Exploratory Medicine and Pharmacology

Associate Director -Clinical Trials Project Manager Exploratory Medicine & Pharmacology Our client, a global pharma company, are currently recruiting for an Associate Director Clinical Trials Project Manager Exploratory Medicine and Pharmacology to join their team on a permanent basis. AsAssociate Director you will lead the creation and execution of the exploratory and biopharmaceutics clinical development and delivery plan, with technical leadership and delivery oversight of clinical research trials within the development plan. Responsibilities ...

Location: Cork,
Associate Director - Clinical Trials Project Manager Exploratory Medicine and Pharmacology 		Cork Not Disclosed

Head of Clinical Research

Head 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. Responsibilities Develop and execute clinical research strategies, plans, and budgets for our product in compliance with regulatory requirements Oversee the design, implementation, and managemen...

Location: Sligo,
Head of Clinical Research 		Sligo Not Disclosed

Associate Director, Clinical Quality & Compliance

Our client is a leading Global Biopharma with a Clinical Trial Centre of Excellence based in Dublin City Centre. They play a crucial role in developing life-saving therapies as they strive to cure unmet medical needs. They are global leaders in the development of therapies in the areas of Infectious Diseases, Oncology & Inflammation. They are looking for an experienced Associate Director with extensive GCP auditing experience to join their Clinical Quality Business Partner team who is ready to dive-in to support their therapeutic areas and clinical development programs. In this ...

Location: Dublin,
Associate Director, Clinical Quality & Compliance 		Dublin Not Disclosed

Associate Director Clinical Trial Capabilities

Associate 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,
Associate Director Clinical Trial Capabilities 		Cork Not Disclosed

Head of Clinical Research

Head 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,
Head of Clinical Research 		Sligo 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