Oncology Clinical Medical Director

Location: San Francisco, CA - USA

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​Our client is a global biotechnology company developing precision, cell-targeting investigational therapies on its technology platform, which utilizes antibodies conjugated with payloads that are specifically activated at the tumor site. They are based in San Francisco and will consider a remote candidate with the requisite experience but will also offer a relocation package if desired.

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They are building their Medical team to support its ongoing and upcoming clinical studies, including a global Phase 3 clinical study. The Medical Director will be a key member of the Medical team with responsibilities to support Medical’s current clinical development program, provide medical expertise to company and project team members, participate as a project team member in new product development and be the medical lead in Phase 1 and Phase 2 trials commensurate with their experience.

Requirements:
The ideal candidate will have an MD, DO, or equivalent degree, hold an active MD &/or DO license, with experience in medical, surgical, or radiation oncology preferred. Additionally, previous industry experience including a working knowledge of drug development process, GCP, ICH guidelines, FDA and EMA regulations as well as direct involvement as an investigator of clinical studies or direct experience in managing clinical operations, medical affairs, and medical safety and monitoring is highly desirable.

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Key Duties and Responsibilities:

• Instruct and oversee investigator’s proper performance of medical therapies

• Provide medical oversight of clinical trials to ensure company standard operating procedures, company directives and regulatory requirements are understood and followed

• Provide medical expertise to identify new product opportunities and portfolio development

• Active participation as a member of the clinical development team for early-stage products

• Medical lead for Phase 1 and Phase 2 clinical trials

• Participate in clinical trial development, including providing input into and/or developing materials such as target product profiles, protocols/amendments and informed consents

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Salary: Excellent salary + Benefits, bonus and stock package