Open role
Medical Affairs Coordinator (IIR)
- Aggregated by CV-Library
- Hampshire
- Temporary
- Full Time
Job Description
Medical Affairs Coordinator
Basingstoke - Contract
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. Interested? Get in touch for further details
Basingstoke - Contract
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. Interested? Get in touch for further details