Offer summary

Qualifications:

Medical Doctor (MD) with a medical thesis preferred., Minimum of 4 years of active clinical practice experience., Experience in the pharmaceutical industry or CRO in medical or project management roles., Understanding of ICH-GCP regulations and familiarity with data visualization systems..

Key responsabilities:

Medically responsible for the trial throughout preparation, conduct, and reporting phases.

Ensure timely preparation of high-quality clinical trial protocols and minimize amendments.

Contribute to trial risk-based quality management and co-author Clinical Quality Monitoring plans.

Perform ongoing reviews of medical data to ensure compliance and quality.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's 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 we're 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.
Co-author 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 ICH-GCP.
Ideally experienced with data visualization systems and IT systems.
*Clinical development/trials experience which would be an additional asset

Required profile