Medical Director/Study Physician - CD Inflammation - Remote - Sponsor Dedicated

Parexel; Uxbridge; On-site; GBP 70,000 - 90,000; Full time

Job summary

Parexel is currently seeking an experienced Study Physician to work in the UK or Germany. You will be medically responsible throughout the preparation, conduct, and reporting phases of clinical trials for key sponsors. This role requires a commitment to maintaining high medical quality.

You should have an MD with relevant specialization and at least 4 years of clinical practice, preferably in medical project management within the pharma industry. Strong knowledge of ICH-GCP regulations is expected.

Qualifications

• Minimum 4 years of active clinical practice experience.
• Specialization in Pulmonology, Immunology, Internal Medicine, or similar.
• Experience in pharmaceutical industry or CRO roles.

Responsibilities

• Medically responsible at the trial level throughout the trial phases.
• Provide medical expertise from trial design to reporting.
• Contribute to trial risk-based quality management.

Skills

Clinical expertise

Medical oversight

Data visualization

Project management

Regulatory knowledge (ICH-GCP)

Education

Physician (MD) with medical thesis

Job description

Parexel is currently seeking an experienced Study Physician to join us in the UK or Germany. 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.

• 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.