Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Study Physician/Medical Monitor - FSP - Hybrid
Job ID R0000030464 , United KingdomParexel is currently seeking an experienced Study Physician to join us in the UK, you be assigned to one of our key sponsors in the EMEA region. The successful applicant is expected to be office based (Bracknell/Reading) for 2 days per week.
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 previous experience as a medical monitor
- Ideally experienced with data visualization systems and IT systems.
- *Clinical development/trials experience which would be an additional asset
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