Senior Clinical Program Manager

Scorpion Therapeutics; California (MO); On-site; USD 164,000 - 205,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Clinical Program Manager to oversee oncology trials, focusing on RAS-targeted programs in late-stage development. You will lead cross-functional teams, ensure GCP/ICH compliance, and manage timelines and budgets across global sites.

The role requires prior clinical operations leadership, with strong experience in oncology and regulatory standards. Travel ~25% and HQ location in Redwood City, CA are expected.

Qualifications

• RN, Bachelor’s, or Master’s in biological sciences or health-related field.
• 10+ years in clinical operations within biotech/pharma, with at least 6 years in study management and leadership.
• Experience in oncology trials and FDA/ICH/GCP regulations.

Responsibilities

• Lead cross‑functional teams to drive trial delivery.
• Ensure trial compliance with GCP, ICH, and SOPs.
• Manage study timelines, budgets, and vendor oversight.

Skills

Clinical operations leadership

GCP/ICH compliance

Budget & timeline management

CRO/vendor oversight

Data analysis & metrics

Education

Bachelor’s degree in biological sciences or health-related field

Master’s degree in related health field

Tools

eTMF

EDC

IRT

CTMS

Job description

Role: Senior Clinical Program Manager responsible for overseeing clinical trials in oncology, particularly focused on RAS-targeted therapies in late-stage development.

Responsibilities

leading cross-functional teams, ensuring trial compliance with GCP, ICH, and SOPs, managing timelines and budgets, vendor oversight (including CROs), and risk management. The role involves developing study documentation, analyzing data metrics, and contributing to strategic planning and SOP development.

Requirements

RN, Bachelor’s, or Master’s in biological sciences or health-related field; 10+ years in clinical operations within biotech/pharma, with at least 6 years in study management and leadership; experience in oncology trials and FDA/ICH/GCP regulations. Preferred: familiarity with eTMF, EDC, IRT, CTMS systems, and experience in early or late-stage oncology development, including international trial operations.

The position may require approximately 25% travel and is based at Revolution Medicines’ headquarters in Redwood City, CA, with a competitive salary range of $164K-$205K.

High-Value: late-stage oncology, RAS inhibitors, clinical trial management, CRO/vendor oversight, international trial experience.