Medical Monitor/Clinical Research Medical Advisor - Remote - FSP
Primary Location: Spain, Remote Additional Locations: Poland, Remote; Romania, Remote; South Africa, Remote ID de la oferta R0000034849 Categoría Medical Sciencessobre este trabajo
Parexel are currently recruiting for an experienced Clinical Research Medical Advisor/Medical Monitor/Study Physician, to join one of a large Sponsor’s in the EU.
This role is accountable for all country clinical/medical aspects of assigned clinical trials, you’ll do this by providing strategic clinical leadership, representing the country specific clinical development function.
Some specifics about this advertised role
- Gather information and provide medical insight for clinical trial concept protocols, ICFs and other clinical documentation.
- Validate study designed and make final decision on the clinical/medical trial and program feasibility of implementing a clinical trial protocol.
- Actively contribute to scientific/clinical/medical aspects of the start up phase.
- Identify and mitigate any challenges to recruitment or clinical data quality
- Provide high calibre indication, compound and protocol training
- Support wider study team partners, acting as the Scientific/Medical expert.
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
What we are looking for in this role
For every role, we look for professionals who have the determination and courage always to put patient well-being first.
That to us is working with heart.
Here are a few requirements specific to this advertised role.
- M.D or Ph.D
- Minimum 3 years experience within clinical development
- In depth understanding of the clinical development process
- Able to communicate with and manage key study stakeholders.
#LI-REMOTE
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