Study PhysicianMedical Monitor - Germany - FSP
Study PhysicianMedical Monitor - Germany - FSP
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Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
Parexel is currently seeking an experienced Study Physician to join us in Germany you be assigned to one of our key sponsors in the EMEA region. This is an upcoming role not an active position.
Working as a Study Physician you will be medically responsible at the trial level throughout the preparation conduct and reporting phase of clinical trial. During the clinical trial you will be responsible to provide medical expertise and medical oversight from the Trial Design Outline to the Clinical Trial Report. This is a core role within the trial team.
Some specifics about this advertised role
- Dedicated to one client.
- Ensure timely preparation of high medical quality clinical trial protocols minimising protocol amendments.
- Contribute to trial risk based quality management by defining medically relevant data and related risks are integrated into the quality and risk management plan.
- Coauthor Clinical Quality Monitoring plans.
- Performing ongoing reviews of medical data.
Here are a few requirements specific to this advertised role.
- Physician (MD) (ideally with medical thesis) trained in a clinical setting and minimum of 4 years of active clinical practice experience; specialization in internal medicine or general practice is desirable.
- Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions/ any other relevant medical function ideally in Clinical Development is desirable.
- Understanding of relevant regulations and guidance including ICHGCP.
- Ideally experienced with data visualization systems and IT systems.
- *Clinical development/trials experience which would be an additional asset
Employment Type
Full Time
