Associate Project Director
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Job Type | Permanent Full Time |
Location | London |
Area | Central London, UK |
Sector | Clinical Research |
Salary | Competitive Salary and Flexible working |
Currency | gbp |
Start Date | ASAP |
Advertiser | remoteapi |
Job Ref | 1093 |
Job Views | 200 |
- Description
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.
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