Job Details

Job Type: Full-time

Salary: $195K - $205K

Location: San Francisco Bay Area

Company Summary: A pre-IPO clinical stage biotech developing therapies to treat cancer and autoimmune disease. Currently they are backed by VCs and have successfully raised nearly a $1 billion continue advancing their clinical programs.

The Opportunity: The AD, Clin Ops will play a critical role in designing and implementing clinical trial protocols. Reporting to the Director, Clinical Science, this person will be responsible for serving as the lea clinical scientist and leading their medical monitoring team in review of clinical data.

Responsibilities:

• Driving scientific execution of clinical protocol by serving as the lead clinical scientist or leading medical monitor team
• Collaborating cross functionally to monitor clinical data to ensure trial quality and completeness
• Ensuring CRF design supports data collection in alignment with protocol
• Applying proficient analytical knowledge and skills to drive program objectives and mitigate risks
• Assisting with generation and presentation of clinical data

An ideal candidate for this role MUST have…

• 10+ years of experience with a Bachelor's degree and 8+ years of experience with a post graduate degree (PhD/PharmD/MD/RN preferred)
• 3+ years of experience within oncology clinical development
• Oncology experience is a MUST
• Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents
• A working knowledge of ICH GCP guidelines

Benefits:

• Pre-IPO biotech company
• Competitive salary with comprehensive benefits (100% medical coverage)
• 401K contribution