Senior Director, Clinical Development- Chronic Weight Management
New
Based in the United StatesFull-TimeDirector
SalaryCompetitive base salary aligned with senior-level clinical development leadership roles in the U.S.
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Job Details
- Experience
- Minimum of 5 years of clinical and/or basic research experience; at least 5 years of leadership or managerial experience.
- Required Skills
- GCP
Requirements
- MD or DO degree from an accredited medical school is required.
- Minimum of 5 years of clinical and/or basic research experience.
- At least 5 years of leadership or managerial experience, including leading teams, programs, or complex projects in a matrix environment.
- Strong background in clinical development within biotech, pharmaceutical, or CRO environments.
- Deep understanding of clinical trial design, biostatistics, and the scientific method applied to medical research.
- Knowledge of Good Clinical Practice (GCP), FDA, EMA/CHMP, and other global regulatory frameworks.
- Proven ability to interpret complex clinical data and translate findings into clear scientific and regulatory communications.
- Strong communication, presentation, and stakeholder engagement skills, with demonstrated scientific credibility in external forums.
- Excellent judgment, problem-solving ability, and the capacity to operate effectively in a complex, fast-paced environment.
Responsibilities
- Support the development, execution, and communication of the global scientific and medical evidence plan, ensuring alignment with clinical and regulatory objectives.
- Provide clinical and scientific expertise to the design, conduct, and interpretation of clinical trials, including safety assessments and data analysis.
- Contribute to regulatory interactions, including preparation of submissions, responses, and participation in meetings with health authorities.
- Author and review key clinical documents such as Clinical Study Reports (CSRs), publications, and regulatory dossiers.
- Build and maintain relationships with key external experts and opinion leaders, including participation in advisory boards and scientific forums.
- Identify and evaluate new clinical research opportunities and support lifecycle management strategies for emerging indications.
- Collaborate cross-functionally with medical, regulatory, safety, and commercial teams to ensure integrated development planning and execution.
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