Study Physician - Remote - Register your interest

Parexel; Greater London; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company is seeking an experienced Study Physician to manage clinical trial responsibilities in the UK. In this role, you will ensure high-quality trial protocols and provide medical oversight during all trial phases. Ideal candidates should have an MD, a minimum of 4 years of clinical practice, and relevant experience in the pharma industry. This position is dedicated to one client and emphasizes risk management and data review.

Qualifications

• Minimum of 4 years of active clinical practice experience.
• Experience in the pharma industry or CRO is desirable.
• Understanding of relevant regulations including ICH-GCP.

Responsibilities

• Medically responsible at the trial level throughout the clinical trial.
• Contribute to timely preparation of high-quality clinical trial protocols.
• Perform ongoing reviews of medical data.

Skills

Clinical expertise

Medical oversight

Risk management

Education

Medical Doctor (MD) with clinical thesis

Specialization in internal medicine or general practice

Tools

Data visualization systems

Clinical trial management systems

Job description

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

Parexel 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. 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