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Clinical Project Manager Part time Options available

Location: Dublin
Experience:5-7 Years
Job Type:Permanent
Salary:Not Disclosed
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Clinical Project Manager Part time options available
Our Dublin based client are currently recruiting for a Clinical Project Manager to join their team on a permanent basis. As 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 Clinical Programs.


  • Develop and execute study plans including setting project goals, risk assessment and management, planning resources and timelines, and study team management
  • Manage performance and development of employees.
  • Manage project-specific training and mentoring
  • Contribute to preparation for audits and inspections as required
  • Evaluate and document investigator and site selection
  • Overall responsibility for management of essential documents and Trial Master File
  • Oversee the process of study initiations, monitoring and close-out
  • Develop and maintain study monitoring plan for the duration of the study lifecycle
  • Review and sign-off initiation, monitoring and close-out reports and documents
  • Participate in process of protocol development
  • Identify issues and manage the resolution process for studies under their supervision
  • Ensure compliance with all applicable SOPs
  • Input in SOP development and updates where appropriate
  • Ensure budget agreements and contracts are in place and roles and responsibilities documented prior to commencing study activities
  • Manage the study budget and associated financial activities for studies under their supervision when applicable
  • Oversee Regulatory and Ethics committee submissions if applicable
  • Confirm the necessary processes are in place for study drug and other supplies for studies under their supervision when applicable
  • Take all reasonable precautions to ensure patient confidentiality is maintained
  • Organise and attend meetings as required
  • Prepare and make presentations as required
  • Update Clinical Program Lead on the status of all clinical trial activities
  • Identification and communication of scientific misconduct
  • Maintain strong relationships with external stakeholders
  • Prepare study reports as required
  • Science and/or medical or nursing background.
  • Minimum of 5 years’ CRA and/or Clinical Project Management experience


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