At a Glance
- Tasks: Coordinate and manage Investigator Initiated Research across international markets.
- Company: Leading global pharmaceutical organisation with a focus on innovation.
- Benefits: Gain valuable experience in clinical research and project management.
- Other info: Dynamic role with opportunities for growth in a global environment.
- Why this job: Make a real impact in the medical field while developing your career.
- Qualifications: 2+ years in clinical research or related fields, with a scientific degree preferred.
The predicted salary is between 40500 - 49500 £ per year.
We're currently recruiting for a Medical Affairs Coordinator to join a leading global pharmaceutical organisation on a contract basis. Working within the International Medical Affairs team, you'll support the coordination and ongoing management of Investigator Initiated Research (IIR) / Investigator Initiated Trials (IITs) across a number of international markets. This is a varied role combining clinical research coordination, project management and stakeholder management, with responsibility for keeping studies on track throughout their lifecycle.
Key responsibilities include:
- Coordinating and tracking investigator-initiated studies from protocol approval through to close-out
- Monitoring study milestones, enrolment, timelines and deliverables
- Supporting contracts, amendments, budgets, invoices and purchase orders
- Liaising with investigators, affiliates and cross-functional internal teams
- Coordinating clinical supply requests and forecasting
- Maintaining accurate study documentation and inspection readiness
- Supporting regulatory documentation and study close-out
- Maintaining study information within systems such as CTMS and internal tracking tools
About you:
We're looking for someone with a background in clinical research, clinical operations, clinical trial coordination or Medical Affairs, ideally with at least 2 years' relevant experience. Experience of clinical study coordination, contracts/budgets, finance or PO processing, working with investigators and cross-functional teams would be particularly valuable. A scientific or health-related degree is preferred, alongside an understanding of clinical drug development and the regulations surrounding medical research.
This could be a great opportunity for a Clinical Trial Associate, Senior CTA, Clinical Project Coordinator, Clinical Operations Associate or Medical Affairs Coordinator looking to broaden their experience within a global pharmaceutical environment.
Medical Affairs Coordinator (IIR) in Basingstoke employer: Entrust Resource Solutions
Entrust Resource Solutions is an excellent employer for R&D Scientists, offering a vibrant work culture in Bradford that fosters collaboration and innovation. With a focus on employee growth, the company provides opportunities for progression and long-term incentives, making it an ideal place for recent PhD graduates to launch their careers in pharmaceutical development.
Contact Details:
Entrust Resource Solutions Recruitment Team
