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Field Medical Director, South Central

ImmunityBio, Inc.
August 23, 2026
Remote friendly (California, United States)
United States
Medical Affairs
Position Summary
The Field Medical Director (FMD) is a field-facing representative of the Medical Affairs Department. Responsibilities include exchanging scientific data and educating health care practitioners on ImmunityBio products and relevant disease states, and facilitating clinical research. The role is non-promotional.

Essential Functions
- Serve as the primary clinical/scientific resource to KOLs and HCPs in assigned geography for disease state and ImmunityBio product/pipeline information.
- Provide accurate, updated clinical/scientific/medical information between KOLs, investigators, and Medical Affairs/Clinical Development.
- Build and maintain peer relationships with KOLs/HCPs.
- Deliver timely clinical/scientific presentations (proactive and in response to requests) in compliance with guidelines and FDA regulatory requirements.
- Identify and report key insights from KOLs/HCPs to Medical Affairs.
- Respond to unsolicited medical information requests; fulfill pharmacovigilance responsibilities.
- Develop and implement the medical territory plan; lead special projects (training materials, MSL training/mentoring, advisory board support).

Training/Education & Research Support
- Maintain deep scientific expertise (oncology/disease states, competitive landscape, products/pipeline, clinical practice, study methodology).
- Support investigator-initiated trials, external collaborations, and HCP-initiated projects; review proposals.
- Support corporate-sponsored trials (site recommendations, site initiation/investigator meeting data presentations, internal communication).

Qualifications
- MD/DO/PhD/PharmD/NP/PA preferred; advanced medical/scientific/clinical degree required.
- Terminal degree strongly preferred.
- 8+ years therapeutic area expertise in oncology/immunology (or relevant to pipeline) required.
- 5+ years in a field-facing liaison role preferred (solid tumors preferred; GU and Lung strongly preferred).
- Clinical trial experience required.
- Valid driver’s license required.

Skills/Abilities
- Knowledge of FDA/OIG, clinical research processes, and treatment guidelines preferred.
- Excellent communication/presentation; strong business acumen; cross-functional and independent work; multitasking; ability to analyze scientific/technical data; proficiency with PowerPoint/Word/Excel; experience with tracking/logging systems.

Working Environment
- Field-based; home-based office; travel ~50% (domestic/international possible); must live in assigned territory; personal vehicle required; MVR check and required auto insurance proof.

Compensation/Benefits & Application
- Discretionary bonus and equity award; base pay range: $214,000–$235,000 (National) or $223,000–$245,000 (Premium markets).
- Benefits include medical/dental/vision, wellness programs, EAP, life/AD&D, short/long-term disability, FSAs, 401(k) match, 529, PTO (incl. 11 holidays; unlimited PTO for exempt).
- Application window: anticipated to close 60 days from posting or sooner if filled/closed.