Location:

San Francisco, CA (Preferred)
Reports to: Director, Clinical Operations
Position Type: Full-Time
Salary Range: $130,000 – $160,000

About Us

At Green Life Science, we are a leading early-stage biotech company focused on oncology therapies. Our Clinical Trial Manager Oncology San Francisco role will help drive two promising Phase I and Phase II oncology clinical trials. We’re building a passionate team committed to clinical excellence and advancing patient outcomes in cancer treatment.

Role Overview: Clinical Trial Manager Oncology San Francisco

As a Clinical Trial Manager specializing in oncology, you will lead the planning, execution, and management of early-phase clinical trials in the San Francisco Bay Area. This role is ideal for someone with a strong oncology clinical trials background who thrives in a fast-paced biotech environment. You will ensure trials meet high-quality, compliance, and timeline standards.

Key Responsibilities of the Clinical Trial Manager Oncology San Francisco

Lead Phase I and II oncology clinical trials, managing study timelines and execution.
Serve as the primary contact for CROs, vendors, and clinical trial sites, ensuring protocol and GCP compliance.
Prepare and maintain critical clinical trial documents, including protocols and informed consent forms.
Oversee site start-up activities, including feasibility assessments, site selection, and contract negotiations.
Collaborate with cross-functional teams such as regulatory, data management, and medical affairs.
Monitor study progress and proactively mitigate risks.
Review clinical data, contribute to study reports, and support regulatory submissions.
Ensure compliance with FDA, ICH-GCP, and ethical standards.
Support the clinical development strategy as oncology programs progress.

Qualifications

Bachelor’s degree in Life Sciences or related field (Master’s preferred).
5+ years’ experience managing clinical trials, with at least 3 years in oncology and early-phase studies.
Experience in startup or small biotech environments is a plus.
Deep understanding of GCP, FDA regulations, and clinical trial operations.
Proven ability to manage CROs and third-party vendors.
Excellent communication, organizational, and problem-solving skills.
Willingness to travel up to 25%.
Ability to work independently within a lean, fast-moving team.

Ready to make a difference in oncology?

Apply today by sending your CV to Alex Smith at:
✉️ alex@greenlsr.com

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