Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job






Salary Expectations:



Current Location:

Notice Period:

Write here your cover note:

If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to

Associate Clinical Project Manager

Reference:SCANGO-616117s Location: Dublin
Republic of Ireland
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed

Associate Clinical Project Manager
Our Dublin based client are currently recruiting for an Associate Clinical Project Manager to join their team on a permanent basis. As Associate 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, lead and coordinate clinical trial activities for assigned studies in line with ICH-GCP and develop and maintain strong working relationships with external stakeholders/Sponsors.


  • Manage and coordinate assigned studies, including review and assessment of study specific documents, development/review and assessment of country specific documents ensuring compliance with ICH-GCP, local regulatory and ethical requirements
  • Oversee/complete regulatory and ethic committee applications where required
  • Primary contact for Sponsor and collaborator groups for assigned studies and groups
  • Provide expertise and feedback to Sponsors and collaborator groups on the regulations and requirements within the assigned countries
  • Share knowledge of country and site-specific processes during the start-up of a trial and throughout to ensure compliance to the protocol can be maintained
  • Manage project-specific training and mentoring of junior staff members as assigned
  • Contribute to preparation for audits and inspections as required
  • Evaluate and document investigator, site and vendor selection as applicable
  • Overall responsibility for management of essential documents and Trial Master File where applicable
  • Responsible for the oversight of study initiations, monitoring and close-out as required for assigned studies
  • Pre-emptively identify potential issues and proactively manage resolutions and put in place, where possible, measures to minimize issues and risk for assigned studies
  • Ensure compliance with all trials you are responsible for
  • Input in SOP development and updates where appropriate
  • Organise, participate in and present at meetings and discussions with other teams and team members
  • Draft and finalise budgets, contracts, and roles and responsibilities prior to commencing study activities
  • Manage the study budget and associated financial activities for assigned studies where applicable
  • Update Head of Clinical Operations and Operations Lead where applicable for assigned studies on the status of all clinical trial activities
  • Prepare study reports and other scientific documents as required

  • Science and/or medical or nursing background
  • Previous Medical or Clinical Research experience, oncology an advantage
  • Proven ability to deliver project goals and mentor junior level employee
  • In-depth knowledge of the Irish clinical trials environment
  • Excellent communication skills with the ability to represent the company at a national level