Parexel
Medical Director/Study Physician - Austria - FSP
Austria · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerParexel
- LocationAustria
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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.
At Parexel FSP, you will be joining a team with a wide variety of experiences and knowledge.
We’re looking for people like you to take the initiative to do things better and smarter people who want to grow personally and professionally.
We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.
Show full description
Parexel is currently seeking an experienced Study Physician to join us in Austria, remotly. You be assigned to one of our key sponsors in the EMEA region.
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.
- +4 years experience as a practicing doctor in a hospital setting, specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, and Emergency Medicine.
- Physician (MD) (ideally with medical thesis)
- 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 previous experience as a medical monitor
- Ideally experienced with data visualization systems and IT systems.
- Clinical development/trials experience which would be an additional assets.
We will offer you
- Premium salary.
- Attractive benefits.
- Medical care plan: Health, Dental & Vision.
- Life Assurance.
- Pension plan
- Excellent work environment.
- Culture of teamwork and collaboration.
- People who motivate and face challenges together.
- Innovative technology.
- Excellent training.
Join a global community where you can transform your career into a life-changing achievement.
Apply directly or contact us via email at marta.kuniewicz@parexel.com
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked
Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.