Back to jobs
POSITION:
Medical Director, Clinical Development
ABOUT THE ROLE:
The Medical Director of Clinical Development guides clinical strategy for key programs and studies. They serve as medical lead and safety physician, closely collaborating with Clinical Operations, Trial Manager, and CRO. This role offers impact and growth in a dynamic organization.
DUTIES AND RESPONSIBILITIES:
- Shape and manage clinical strategy for programs.
- Monitor clinical studies, ensuring patient safety and data interpretation.
- Develop scientific methods for protocols, data systems, and reports.
- Lead clinical development plans and strategies.
- Draft trial protocols, coordinating cross-functional teams.
- Collaborate with pre-clinical, translational sciences, and management.
- Lead cross-functional product teams.
- Assist in site/investigator selection and CRO management.
- Supervise project team, manage trial budgets.
- Maintain SOP and GCP compliance.
QUALIFICATIONS:
- Medical Doctor (MD) required, Neurology/Psychiatry experience preferred.
- 3-5+ years in CRO/pharma/biotech, GCP knowledge.
- 3+ years CNS clinical research, protocol drafting experience.
- Safety physician expertise, narrative drafting.
- Strong communication skills across diverse stakeholders.
- Analytical, thrives in fast-paced environments.
LANGUAGE:
- Fluent in English and French
WORK ENVIRONMENT:
- Location: Paris
- Hybrid: 3 days office, 2 days from home
Medical Director - France
- Location France
- Salary Negotiable
- Discipline Clinical Development
- Reference PR/450000_1693400471
Medical Director, Clinical Development
ABOUT THE ROLE:
The Medical Director of Clinical Development guides clinical strategy for key programs and studies. They serve as medical lead and safety physician, closely collaborating with Clinical Operations, Trial Manager, and CRO. This role offers impact and growth in a dynamic organization.
DUTIES AND RESPONSIBILITIES:
- Shape and manage clinical strategy for programs.
- Monitor clinical studies, ensuring patient safety and data interpretation.
- Develop scientific methods for protocols, data systems, and reports.
- Lead clinical development plans and strategies.
- Draft trial protocols, coordinating cross-functional teams.
- Collaborate with pre-clinical, translational sciences, and management.
- Lead cross-functional product teams.
- Assist in site/investigator selection and CRO management.
- Supervise project team, manage trial budgets.
- Maintain SOP and GCP compliance.
QUALIFICATIONS:
- Medical Doctor (MD) required, Neurology/Psychiatry experience preferred.
- 3-5+ years in CRO/pharma/biotech, GCP knowledge.
- 3+ years CNS clinical research, protocol drafting experience.
- Safety physician expertise, narrative drafting.
- Strong communication skills across diverse stakeholders.
- Analytical, thrives in fast-paced environments.
LANGUAGE:
- Fluent in English and French
WORK ENVIRONMENT:
- Location: Paris
- Hybrid: 3 days office, 2 days from home