Associate Project Director - Clinical Research - London or Remote 

As the Associate Project Director, you'll be responsible for the overall coordination and management of clinical trials from start-up through to close and line managing the project management team.

You will lead cross-functional teams to identify/mitigate/escalate project issues and ensure solutions are implemented and be accountable for all project deliverables.

Specific tasks would include:

• Assigned to manage a full range of projects;
• Attend and present at client bid-defense meetings.
• Prepares proposals, budgets and addendums.
• Interacts with clients and company vendors to ensure that all contractual obligations are met.
• Identifies potential bottlenecks and/or delays; develops and executes contingency plans in order to keep the project on schedule.
• Ensures adequate resource requirements.
• Develops Project Management Plan to include timeline and milestones.
• Coordinates Project Team Meetings, including development of meeting agendas and minutes.
• Coordinates study specific training and other requirements for internal and external staff, as appropriate.
• Manages budget throughout the duration of the project and develops out of scope documentation and costs.
• Ensures knowledge of clinical research, clinical therapeutics and regulatory issues, is current through review of journal articles and attendance of relevant professional association meetings.
• Contributes to the development and revision of Standard Operating Procedures - (SOPs) and departmental policies.
• May participate in the analysis and development of Project Management Department budgets.

What our client likes to see:

• Bachelor / Master degree, in a related field of study and 10 years applicable industry experience or equivalent combination of education and experience required.
• Experience as a clinical Project Manager is required (CRO experience preferred).
• Experience of complete Project management from start-up to close out
• A very good understanding of project management techniques.
• Working knowledge of GCPs, ICH guidelines, FDA and other applicable country regulations.
  
  
  

#pharmajobs #projectmanagement #agile #cro #pharma #PM #Projectmanager #scrum #lifescience