Clinical Research Physician - Oncologist

Medpace; Greater London; Presencial; GBP 80.000 - 100.000; Tempo integral

Resumo da vaga

A leading clinical research organization is seeking a Clinical Research Physician - Oncologist. This role requires an M.D. degree and experience in clinical trials. Responsibilities include medical management of trials, contributing expertise to study documentation, and ensuring safety in trials. You will be a key player in new clinical projects, guiding design and execution with a team of professionals. The ideal candidate has strong background in oncology with board certification and is proficient in the pharmaceutical industry.

Qualificações

• Must have an M.D. degree or equivalent with board certification preferred.
• Prior clinical trial research experience preferred.
• Experience in pharmaceutical-related clinical research preferred.

Responsabilidades

• Provide medical management and expertise for clinical trials.
• Contribute medical expertise to study reports and regulatory documents.
• Manage safety issues in clinical trials.

Conhecimentos

Medical management expertise

Clinical trial knowledge

Safety issue management

Formação

M.D. degree or equivalent

Board certification

Descrição da vaga

Clinical Research Physician - Oncologist

We are seeking a Medical Director - Oncology/Solid tumor to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required.

Responsibilities

• Provide medical management and expertise for clinical trials
• Contribute medical expertise to study reports, regulatory documents, and manuscripts
• Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials
• Participate in new business development through involvement in proposal and sponsor meetings as requested
• Coordinate with other departments in all phases of the studies and trials, including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents
• Follow specific research related protocol and lead others in strict adherence to the policies

Qualifications

• Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred
• Prior clinical trial research experience preferred
• Previous experience in pharmaceutical-related clinical research is preferred

Travel: up to 20%

About Medpace

Medpace is a full-service clinical contract research organization (CRO) that provides Phase I‑IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. Medpace is headquartered in Cincinnati, Ohio, employs more than 5,000 people across 40+ countries.