At a Glance
- Tasks: Lead clinical trials and provide medical expertise to improve patient health.
- Company: Join Parexel, a leader in clinical development with a mission to enhance global health.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Be part of a dedicated team focused on high-quality clinical trial protocols.
- Why this job: Make a real difference in patients' lives while working on innovative therapies.
- Qualifications: MD with 4+ years of clinical experience; specialization in relevant fields preferred.
The predicted salary is between 80000 - 100000 £ per year.
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 the UK or Germany. You will 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 trials. During the clinical trial, you will be responsible for providing 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 integrated into the quality and risk management plan.
- Co-author Clinical Quality Monitoring plans.
- Perform 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 Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, and Emergency Medicine is highly 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.
Medical Director/Study Physician - CD Inflammation - Remote - Sponsor Dedicated employer: Parexel
At Parexel FSP, we pride ourselves on being an exceptional employer, offering a dynamic and supportive work environment for our IRT Vendor Start-up Manager role. With a focus on employee growth and development, we provide comprehensive training and opportunities to collaborate with industry experts, all while enjoying the flexibility of a home-based position in the UK or Ireland. Our commitment to excellence and innovation ensures that you will be part of a team that values your contributions and fosters a culture of success.
