Senior Clinical Program Manager, Clinical Operations

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit high-value frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding scientists in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

This is a unique opportunity for a Clinical Operations Professional who has technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP), and U.S. Food and Drug Administration (FDA) regulatory requirements. Oncology experience preferred. As the Clinical Program Manager/Sr. Clinical Program Manager of Clinical Operations, initially reporting to the Associate Director/Director Clinical Operations, you will be responsible for Contract Research Organization (CRO) oversight and execution of Revolution Medicines clinical studies.

Responsibilities:

• Clinical operations functional activities related to the execution of assigned clinical programs based upon department and corporate goals and objectives.

• Management of clinical studies and vendors to ensure studies are completed on time, within budget, and in compliance with Standard Operating Procedures (SOPs), FDA regulations, and International Council for Harmonization (ICH)/ GCP guidelines.

• Identify, engage, and manage the activities of clinical CROs and other clinical study providers (e.g., core labs, Electronic Data Capture (EDC) provider, and independent contractors) to execute clinical trials.

• Reviewing and contributing to the development of study-specific documentation including clinical trial protocols, case report forms, study guides/manuals, informed consent forms, and clinical databases.

• Reviewing monitoring reports and other study documentation as required.

• Oversight of the collection and management of clinical trial documentation to be filed in the Trial Master File (TMF).

• Participation in team meetings and collaboration with other functional groups within the company (e.g., Clinical Development, Pharmacokinetics, Quantitative Sciences, Regulatory, QA, Finance, Legal, etc.) to achieve clinical study goals.

• Following up on assigned team action items and identification, escalation, and resolution of issues as needed.

• Collaboration with contracts specialists to review and negotiate Clinical Trial Agreements and site-specific study budgets.

• Assessment of adequacy/feasibility of potential clinical investigators and sites including evaluating facilities, personnel, patient referral base, and adherence to GCP.

• Development of clinical study monitoring priorities and Monitoring Plan in conjunction with CRO.

• Conduct site visits (e.g., training visits, site initiation visits, monitoring visits), as required.

• Managing investigational product accountability and reconciliation process.

• Assistance with the preparation of safety, interim, and final clinical study reports, and resolution of data discrepancies.

• Providing clinical trial support, mentoring, leadership, guidance, and direction to Clinical Research Associates (CRAs) assigned to clinical studies.

• Preparation and tracking of study participant enrollment projections vs. actuals and study budgets.

• Serving as a primary clinical operations contact for internal and external (clinical sites, vendors, etc.) teams for assigned studies.

Required Experience, Skills, and Education:

• BS or MS degree with a minimum of 8 years of clinical operations experience in the pharmaceutical or biotech industries.

• Direct experience in running early-stage clinical trials within an industry environment.

• Strong working knowledge of FDA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials.

• Experience in the selection of CROs/ vendors and management of external resources.

• A demonstrable record of strong vendor management and teamwork.

• Direct experience in managing clinical CROs.

• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.

• Excellent written and verbal communication skills.

• Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team.

• Ability to travel (~25%).

Preferred Skills: 

• Experience with Oncology clinical trials.

• Experience in working with cooperative group studies and investigator-sponsored trials.

• Experience in clinical trial operations outside the USA is desirable.

• Knowledge of APAC region.

The expected salary range for this role is $150,000 to $190,000.  An individual’s position within the range may be influenced by multiple factors, including skills and experience in role, overall performance, individual impact and contributions, tenure, and market dynamics. Base salary is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.