At a Glance
- Tasks: Lead and execute clinical development strategies and oversee trial protocols.
- Company: Leading pharmaceutical company with a focus on innovation.
- Benefits: Competitive daily rate, hybrid working, and collaborative environment.
- Other info: Opportunity for professional growth in a dynamic, cross-functional team.
- Why this job: Shape clinical strategy and make a real impact in global health.
- Qualifications: Extensive experience in clinical development and strong leadership skills.
Type: Temporary
Duration: 6 months
Location: London (hybrid working available)
Rate: (INSIDE IR35) up to 480 per day (PAYE)
We are working with a leading pharmaceutical company who are seeking an experienced Clinical Development Director to provide scientific and clinical leadership across global clinical development programs and studies. This role will play a pivotal part in shaping clinical strategy, driving high-quality trial execution, and ensuring the successful delivery of clinical and regulatory milestones within a collaborative, cross-functional environment.
Key Responsibilities
- Lead and support the development and execution of clinical development strategies, clinical trial protocols, and other key clinical deliverables.
- Drive clinical data review, analysis, and interpretation, contributing to study reports, publications, and scientific presentations.
- Author and oversee clinical sections of regulatory submissions, investigator brochures, briefing documents, safety updates, and responses to regulatory authorities.
- Collaborate with cross-functional teams including medical, biostatistics, data management, regulatory affairs, and safety to ensure high-quality clinical trial delivery.
- Support safety monitoring activities and contribute to risk management and safety reporting throughout the development lifecycle.
- Engage with external experts, regulatory agencies, advisory boards, and others.
We think you need these skills to ace Clinical Development Director
Clinical Development Strategy
Clinical Trial Protocols
Data Review and Analysis
Regulatory Submissions
Collaboration with Cross-Functional Teams
Safety Monitoring
Risk Management
