Medical Science Liaison, Oncology - Southern CA
Corcept Therapeutics
August 14, 2026
On-site
Los Angeles, CA
Medical Affairs
Responsibilities:
- Model and promote key principles: collaborating effectively, embracing possibilities, following the data, and leading by doing.
- Engage in clinically meaningful scientific discussions with thought leaders and HCPs in gynecological oncology and other malignancies to enhance knowledge of Corcept and glucocorticoid receptor antagonism in oncology.
- Support products via HCP communication and education through scientific presentations and education.
- Respond to medical inquiries from HCPs in a timely and scientifically accurate manner.
- Conduct scientific exchange on non-clinical/clinical trial data; consistently ask thoughtful questions and challenge stakeholders.
- Develop and maintain strong relationships with thought leaders, patient advocacy organizations, and oncology associations (e.g., GOG, ASCO, regional organizations).
- Capture, analyze, and communicate compliant insights and intelligence to inform decisions.
- Support sponsored clinical trials, investigator-initiated studies (IIS), publications, clinical/scientific education, advisory boards, and congresses.
- Maintain high scientific/clinical/technical expertise; critically review literature and provide evidence-based insights.
- Collaborate cross-functionally with Clinical Development, Clinical Operations, Market Access, Marketing, Commercial, Data Analytics, etc.
- Attend medical conferences and events; strategically identify KOLs for advisory boards.
- Maintain territory plan and adapt to changes.
- Travel 50–70%.
Qualifications / Preferred Skills:
- Strong oncology acumen (e.g., therapeutic landscapes, NCCN guidelines, clinical trial data, cooperative groups, NCI/NCCN cancer centers).
- Core competencies: intellectual curiosity, managing change, teamwork, communication, achieving results, decision-making, clinical/scientific expertise.
- Business acumen across drug development functions (clinical development/ops, biostatistics, regulatory, commercial, etc.).
- Project management skills; prioritize and ensure on-target, within-budget delivery.
- Experience with PowerPoint, Word, and Excel; create/edit accurate content.
- Experience with Veeva CRM/Vault preferred; SharePoint and/or BOX preferred.
- Driving record maintained per company vehicle policy.
Preferred Education/Experience:
- Advanced degree in clinical/medical science (PhD, MD, PharmD, MSN, PA, NP) required.
- 1–3+ years MSL experience; 2+ years oncology experience.
Application Instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.
- Model and promote key principles: collaborating effectively, embracing possibilities, following the data, and leading by doing.
- Engage in clinically meaningful scientific discussions with thought leaders and HCPs in gynecological oncology and other malignancies to enhance knowledge of Corcept and glucocorticoid receptor antagonism in oncology.
- Support products via HCP communication and education through scientific presentations and education.
- Respond to medical inquiries from HCPs in a timely and scientifically accurate manner.
- Conduct scientific exchange on non-clinical/clinical trial data; consistently ask thoughtful questions and challenge stakeholders.
- Develop and maintain strong relationships with thought leaders, patient advocacy organizations, and oncology associations (e.g., GOG, ASCO, regional organizations).
- Capture, analyze, and communicate compliant insights and intelligence to inform decisions.
- Support sponsored clinical trials, investigator-initiated studies (IIS), publications, clinical/scientific education, advisory boards, and congresses.
- Maintain high scientific/clinical/technical expertise; critically review literature and provide evidence-based insights.
- Collaborate cross-functionally with Clinical Development, Clinical Operations, Market Access, Marketing, Commercial, Data Analytics, etc.
- Attend medical conferences and events; strategically identify KOLs for advisory boards.
- Maintain territory plan and adapt to changes.
- Travel 50–70%.
Qualifications / Preferred Skills:
- Strong oncology acumen (e.g., therapeutic landscapes, NCCN guidelines, clinical trial data, cooperative groups, NCI/NCCN cancer centers).
- Core competencies: intellectual curiosity, managing change, teamwork, communication, achieving results, decision-making, clinical/scientific expertise.
- Business acumen across drug development functions (clinical development/ops, biostatistics, regulatory, commercial, etc.).
- Project management skills; prioritize and ensure on-target, within-budget delivery.
- Experience with PowerPoint, Word, and Excel; create/edit accurate content.
- Experience with Veeva CRM/Vault preferred; SharePoint and/or BOX preferred.
- Driving record maintained per company vehicle policy.
Preferred Education/Experience:
- Advanced degree in clinical/medical science (PhD, MD, PharmD, MSN, PA, NP) required.
- 1–3+ years MSL experience; 2+ years oncology experience.
Application Instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.