Medical Director, Clinical Development, Obesity

Responsibilities

• Acts as medical expert and leader in interactions with external stakeholders
• Defines clinical trial-related Clinical Development Program (CDP) goals and objectives
• Works closely with discovery teams to provide input on the next generation of targets in the field
• Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts
• Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings
• Leads the Global Clinical Study Team to produce high quality program deliverables on schedule
• Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety

Requirements

• An M.D. or equivalent with board eligibility or board certification in Pediatric Endocrinology preferred; relevant experience can be acceptable.
• At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)
• Experience in metabolic disorders drug development strongly preferred
• Previous interactions with regulatory agencies or common technical document (CTD or dossier) submission in an ICH region is an advantage

Qualifications

A qualified physician with pharmaceutical industry experience, preferably in the area of metabolism, in relevant areas such as obesity or Type 2 diabetes.

Skills

High-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.

Benefits

Not specified

Pay

$284,900.00 - $385,700.00 annually

Schedule

Full time