Director, Oncology Clinical Affairs (MD)
Corcept Therapeutics
August 17, 2026
Remote friendly (United States)
United States
Medical Affairs
Responsibilities
- Partner with Medical Affairs leadership to execute medical priorities for product adoption and long-term integration into clinical practice; serve as the clinical bridge between Clinical Development and go-to-market.
- Provide clinical and scientific expertise for medical affairs priorities, tactical planning, internal training, advisory boards, congress activities, and cross-functional initiatives.
- Identify unmet medical need and translate scientific insights into practical clinical guidance.
- Lead peer-to-peer scientific interactions with oncology experts, KOLs, researchers, academic centers, and external medical stakeholders.
- Engage physicians via advisory boards, congress interactions, speaker preparation, and insight-gathering to inform medical strategy, education, publications, and evidence planning.
- Provide clinical input to post-approval evidence generation (RWE, ISS, registries) and review ISS proposals.
- Evaluate scientific/clinical data and emerging practice trends to inform internal strategy and external communications.
- Support development of accurate, balanced, compliant medical/educational information and promotional review materials.
- Interpret and influence guideline updates and treatment pathways (e.g., NCCN, ASCO) and translate changes into clinical and business implications.
- Partner with Market Access and HEOR; participate in payer-facing discussions requiring deep clinical expertise.
- Partner with Pharmacovigilance and Clinical Development to develop safety guidance; translate safety data into clinician-facing recommendations and supportive care guidance.
Qualifications / Skills
- MD required.
- Oncology experience required; gynecologic oncology preferred.
- 3–5+ years of relevant oncology practice (including fellowship).
- Demonstrated ability to evaluate clinical evidence, evolving treatment pathways, and oncology trends; strong oral/written/presentation skills.
- Collaborative, cross-functional leadership with sound judgment and scientific rigor.
- Ability to travel 25–30% (or as needed).
Application instructions
- Must be currently authorized to work in the United States on a full-time basis.
- Partner with Medical Affairs leadership to execute medical priorities for product adoption and long-term integration into clinical practice; serve as the clinical bridge between Clinical Development and go-to-market.
- Provide clinical and scientific expertise for medical affairs priorities, tactical planning, internal training, advisory boards, congress activities, and cross-functional initiatives.
- Identify unmet medical need and translate scientific insights into practical clinical guidance.
- Lead peer-to-peer scientific interactions with oncology experts, KOLs, researchers, academic centers, and external medical stakeholders.
- Engage physicians via advisory boards, congress interactions, speaker preparation, and insight-gathering to inform medical strategy, education, publications, and evidence planning.
- Provide clinical input to post-approval evidence generation (RWE, ISS, registries) and review ISS proposals.
- Evaluate scientific/clinical data and emerging practice trends to inform internal strategy and external communications.
- Support development of accurate, balanced, compliant medical/educational information and promotional review materials.
- Interpret and influence guideline updates and treatment pathways (e.g., NCCN, ASCO) and translate changes into clinical and business implications.
- Partner with Market Access and HEOR; participate in payer-facing discussions requiring deep clinical expertise.
- Partner with Pharmacovigilance and Clinical Development to develop safety guidance; translate safety data into clinician-facing recommendations and supportive care guidance.
Qualifications / Skills
- MD required.
- Oncology experience required; gynecologic oncology preferred.
- 3–5+ years of relevant oncology practice (including fellowship).
- Demonstrated ability to evaluate clinical evidence, evolving treatment pathways, and oncology trends; strong oral/written/presentation skills.
- Collaborative, cross-functional leadership with sound judgment and scientific rigor.
- Ability to travel 25–30% (or as needed).
Application instructions
- Must be currently authorized to work in the United States on a full-time basis.