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

GCP/Pharmacovigilance Inspector

Our client is regulatory authority who are based in Dublin. They are seeking a GCP/ Pharmacovigilance Inspector to join an established team on a 2 year contract. Reporting to the GCP/Pharmacovigilance Inspection Manager, the role of an Inspector is to evaluate the compliance of sites inspected, both in Ireland and internationally, with the requirements of National legislation (in Ireland), European community directives, regulations and guidance. These include: Hospitals, Clinics, healthcare centres, clinical research facilities, sponsor organisations, CROs, C...

Location: Dublin,
GCP/Pharmacovigilance Inspector
Dublin Not Disclosed

Clinical Trials Associate Fluent Italian (based in Ireland)

Clinical Trials Associate Fluent Italian (based in Ireland) Our Cork based client are currently recruiting for an experienced fluent Italian speaking Clinical Trials 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 clin...

Location: Cork,
Clinical Trials Associate Fluent Italian (based in Ireland)
Cork Not Disclosed

Clinical Trials Associate Fluent Spanish (based in Ireland)

Clinical Trials Associate Fluent Spanish (based in Ireland) Our Cork based client are currently recruiting for an experienced fluent Spanish speaking Clinical Trials 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 clin...

Location: Cork,
Clinical Trials Associate Fluent Spanish (based in Ireland)
Cork Not Disclosed

Senior Director, Clinical Operations

Our client is a leading Biopharma who are establishing a Centre of Excellence in Dublin for their Global Development & Clinical Operations. The Senior Director, Clinical Operations will be a key member of the Dublin Leadership Team and will closely partner with Department Heads of each Therapeutic Area within the organization. The successful candidate will be a valued member of therapeutic area leadership and life cycle management teams. In addition, he/she will provide clinical operational strategy and oversight of multiple compounds, indications, and programs to ensure ...

Location: Dublin,
Senior Director, Clinical Operations
Dublin Not Disclosed

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, Pharmacovigilance Quality & Compliance (GVP)

Our client is a leading Global Biopharmaceutical organisation who play a crucial role in developing life-saving therapies. They are seeking a Pharmacovigilance Compliance Director who will join their Global R&D Quality and Compliance team. As a member of the global PV management team you will provide leadership in setting the strategic direction of Quality and Compliance PV activities. This role is suited to candidates who possess strong leadership skills and strategic thinking. Utilizing expert Good Pharmacovigilance (GVP) and Good Clinical Practice (GCP) knowledge. The su...

Location: Dublin,
Director, Pharmacovigilance Quality & Compliance (GVP)
Dublin 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)

Clinical Trial Associate German Speaking (based in Ireland) Our Cork based client are currently recruiting for an experienced fluent German speaking Clinical

Location: Cork,
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