Hendre Moolman is recruiting for a Senior Project Manager to join a successful, global pharmaceutical company. The role will be office based at their site in Hertfordshire.
The main purpose of the role will be to:
As a Senior Project Manager, you will project manage all aspects of the implementation of the EMA Clinical Trial Regulation for both new studies and ongoing studies.
The role will work closely with the committee to ensure all decisions are implemented and actioned items are complete.
The role will be responsible for drafting and maintaining the cross functional project plan for implementation and transition, identifying key activities, stakeholders, and owners, and driving all activities to completion.
You will work closely with the leaders of the Clinical Trial Regulation Forum sub teams to support decision making and planning.
To succeed in this role, you will come from a Life Science background with demonstrable project management experience in the pharmaceutical industry:
- Project Management qualifications such as PRINCE2 would be advantageous
- Previous experience working a GCP/Regulatory/Drug Development (Clinical Development) environment is an advantage
- Previous experience within change management is an advantage
For more information or to apply for this position, please contact Hendre Moolman on 01438 842 970 or email firstname.lastname@example.org.
Entitlement to work in the UK is essential for this role.