Senior Study Physician | Medical Oversight for Trials

Parexel; England; Presencial; GBP 75 000 - 105 000; Tempo integral

Resumo da oferta

Parexel is seeking an experienced Study Physician to join us in the UK or Germany. You will be medically responsible at the trial level throughout preparation, conduct and reporting phases, providing medical oversight from the Trial Design Outline to the Clinical Trial Report.

This core role supports one client within our global clinical development team, contributing to high-quality protocols and risk-based quality management.

Qualificações

• Physician (MD) with minimum of 4 years of active clinical practice.
• Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine is highly desirable.
• Understanding of ICH-GCP regulations.
• Ideally previous experience as a medical monitor.
• Experience with data visualization systems and IT systems is a plus.

Responsabilidades

• Dedicated to one client.
• Ensure timely preparation of high quality clinical trial protocols, minimising protocol amendments.
• Contribute to trial risk-based quality management by defining medically relevant data and risks in quality and risk management plans.
• Co-author Clinical Quality Monitoring plans.
• Performing ongoing reviews of medical data.

Conhecimentos

MD

4+ years clinical practice

Pulmonology

Immunology

Internal Medicine

Infectious Diseases

Family Medicine

Pediatrics

Rheumatology

Emergency Medicine

Medical monitor experience

Data visualization IT systems

Formação académica

MD degree

Ferramentas

Data visualization systems

IT systems

Descrição da oferta de emprego

Parexel is seeking an experienced Study Physician to join us in the UK or Germany. You will be medically responsible at the trial level throughout preparation, conduct and reporting phases, providing medical oversight from the Trial Design Outline to the Clinical Trial Report.

This core role supports one client within our global clinical development team, contributing to high-quality protocols and risk-based quality management.