Clinical Trial Manager

Green Life Science; San Francisco (CA); On-site; USD 130,000 - 160,000; Full time

Job summary

An innovative early-stage biotechnology company is seeking a Clinical Trial Manager to lead oncology trials. This role involves managing complex studies from start to finish, ensuring compliance with regulatory standards, and collaborating with cross-functional teams. Join a dynamic team dedicated to advancing transformative oncology therapies and make a real impact on cancer patient outcomes. If you thrive in fast-paced environments and have a passion for clinical excellence, this opportunity is perfect for you.

Benefits

Competitive Compensation

Equity Participation

Comprehensive Benefits Package

Opportunity to Work on Cutting-Edge Programs

Qualifications

• 5+ years of clinical trial management experience, including oncology.
• Strong knowledge of ICH-GCP and FDA regulations.

Responsibilities

• Manage all aspects of assigned clinical trials ensuring timelines and quality.
• Serve as primary contact for CROs and oversee their performance.
• Monitor trial progress and implement risk mitigation strategies.

Skills

Clinical Trial Management

Oncology Expertise

Regulatory Compliance (ICH-GCP, FDA)

Project Management

Vendor Management

Communication Skills

Problem-Solving Skills

Team Coordination

Education

Bachelor's Degree in Life Sciences

Advanced Degree (Preferred)

Job description

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Job Title: Clinical Trial Manager – Oncology

Reports to: Director Clinical Operations

Position Type: Full-time

Salary Range: $130,000 - $160,000

Company Overview:

Our Biotech are an innovative, early-stage biotechnology company dedicated to advancing transformative oncology therapies. With two assets currently in Phase I and Phase II clinical development, we are building a dynamic team committed to rigorous science, clinical excellence, and improving outcomes for cancer patients.

Position Summary:

We are seeking a highly motivated and experienced Clinical Trial Manager (CTM) to lead the execution of our early-phase oncology clinical trials. The ideal candidate will have hands-on experience in managing complex oncology studies from start-up through completion and thrive in a fast-paced, cross-functional biotech environment. This role will be instrumental in driving clinical trial strategy and execution in alignment with regulatory and operational standards.

Key Responsibilities:

• Manage all aspects of assigned clinical trials (Phase I–II) including planning, execution, and oversight, ensuring timelines, budgets, and quality standards are met.
• Serve as the primary point of contact for CROs, vendors, and clinical sites; oversee their performance and ensure adherence to protocols and GCP.
• Develop and maintain study documentation (protocols, investigator brochures, ICFs, CRFs, monitoring plans, etc.).
• Lead site start-up activities including feasibility assessments, site selection, and contract/budget negotiation.
• Coordinate cross-functional teams (clinical operations, data management, regulatory, medical, and pharmacovigilance) to support trial execution.
• Monitor clinical trial progress, proactively identify risks, and implement mitigation strategies.
• Participate in the review of clinical data and contribute to clinical study reports and regulatory submissions.
• Ensure compliance with all regulatory and ethical requirements including ICH GCP and FDA regulations.
• Provide input on clinical development plans and contribute to long-term strategy as the company advances assets through development stages.

Qualifications:

• Bachelor's degree in life sciences or related field (advanced degree preferred).
• 5+ years of clinical trial management experience, including at least 3 years in oncology and early-phase trials.
• Prior experience in a small biotech or startup environment preferred.
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes.
• Demonstrated ability to manage CROs and third-party vendors effectively.
• Proven ability to work independently in a fast-paced, lean team setting.
• Excellent organizational, communication, and problem-solving skills.
• Willingness to travel as needed (up to 25%).

Why Join Us?

• Opportunity to work on cutting-edge oncology programs with high potential.
• Collaborative, entrepreneurial culture where your contributions make a real impact.
• Competitive compensation, equity participation, and comprehensive benefits package.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science, Research, and Health Care Provider

• Industries

  Biotechnology Research, Pharmaceutical Manufacturing, and Hospitals and Health Care

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