Medical Director, Endocrinology

The Medical Director will represent Corcept to the highest ethical and professional standards and in accordance with guidelines, directions, and policies. The Medical Director will be aligned with the mission, vision, and values of the Medical Affairs Team. This role will lead real-world data generation and support Investigator-Initiated Studies (IIS). Additionally, the Medical Director will support KOL identification and engagement, manuscript development, data generation planning, and overall strategy and execution.

Responsibilities:

• Collaborate cross-functionally with Clinical Development, Medical Affairs, Pharmacovigilance, Market Access, and Commercial teams to define late-phase data needs
• Develop and implement data generation strategies to support evidence-based decision-making
• Translate data generation strategy into clinical trial outlines and protocols
• Lead the Registry and support IIS, including planning, execution, and management
• Medical Monitor for Real-World data generation, and partner with an external CRO to ensure studies are executed in compliance with GCP, ICH, and local regulatory requirements
• Collaborate with investigators and study sites to support study execution and data collection
• Analyze and interpret study results in the context of clinical practice and real-world patient populations
• Develop and implement KOL engagement plans to support medical and scientific initiatives
• Facilitate scientific discussions and collaborations with KOLs to advance knowledge and advocacy for Corcept’s products and disease areas
• Support data dissemination through peer-reviewed publications, congress presentations, and medical education initiatives
• Contribute to the development and execution of Medical Affairs strategies and plans
• Collaborate with cross-functional teams to ensure alignment and successful implementation of strategies
• Maintain the highest standards of scientific, clinical, and technical expertise in relevant therapeutic areas
• Travel required, up to 20%

Preferred Skills, Qualifications and Technical Proficiencies:

• Proven experience designing and executing real-world data generation and post-marketing studies in compliance with FDA standards
• Familiarity with real-world data sources (claims, EHR, registries, digital health data), data linkage and data-governance, and analytical methodologies
• Experience in developing and implementing data generation strategies
• Experience managing CROs to ensure study quality, timeliness, and compliance
• Proven ability to build and maintain relationships with key opinion leaders (KOLs), investigators, academic networks and external research organizations to identify unmet clinical/data needs and study opportunities
• Ability to think strategically and demonstrated troubleshooting and problem-solving skills
• Exceptional project management and organizational skills
• Excellent interpersonal and communication skills
• Demonstrates a strong ability to collaborate with cross-functional teams to achieve common goals and drive project success
• Possesses excellent oral presentation skills and is adept at working independently with scientific and technical personnel, ensuring clear and effective communication
• Thrives in a fast-paced setting, capable of adjusting workload and priorities based on changing demands with minimal direction

Preferred Education and Experience:

• D. or D.O., specialized in Endocrinology or Cardiometabolic disease, is required
• 12 years of experience, including at least 4 years in clinical trial management or drug development
• Proven track record in designing and overseeing late-phase or RWE studies from concept through publication

The pay range that the Company reasonably expects to pay for this position is $238,400 - $315,600; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

Applicants must be currently authorized to work in the United States on a full-time basis.