Job Description

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit 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:

As a Clinical Trial Assistant II in Clinical Operations, initially reporting to the Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials.

Assisting in the development, review, distributing, and archiving of study specific documents and reports (plans, training materials, study guides, manuals, etc.)

Assisting with updating and maintaining clinical systems and any reporting tools.

Set up and maintenance of the trial master files (TMF) if applicable, or work with CRO to audit and resolve discrepancies.

Create, maintain, and track information for key study related activities.

Assisting in the preparation of meeting materials, scheduling meetings, and developing agendas, taking meeting minutes for internal clinical operation team meetings

Gathering investigator and site information, to support study start-up, maintenance and close out activities.

Working with cross functional study teams, and vendors to assist in the coordination of clinical trial activities.

Support other clinical operations activities as appropriate.

Required Experience, Skills, and Education:

Bachelor’s degree in biological sciences or related health related field required.

1 - 3 years of relevant experience in the pharmaceutical or biotech industry, preferably in clinical operations or clinical research-related experience.

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

Excellent written and verbal communication skills.

Demonstrate proficiency in Microsoft Word, Excel and PowerPoint and other software platforms.

Demonstrated ability to multi-task, prioritize options.

Travel up to (~25%).

Preferred Skills:

Preferably in clinical operations or clinical research-related experience.

Experience in oncology clinical trials.

The base salary range for this full-time position is $75,000 to $90,000 for candidates working onsite at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the salary for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that 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.

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