Clinical Trial Assistant at Revolution Medicines

Redwood City, California, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Jul, 26

Salary

108000.0

Posted On

22 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical operations, Clinical trial management, Trial master files, Study start-up, Regulatory documentation, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Communication skills, Project coordination, Data management, Vendor management, Oncology, Clinical research

Industry

Hospitals and Health Care

Description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: This is a unique opportunity for an entry-level Clinical Operations Professional. The Clinical Trial Assistant of Clinical Operations, initially reporting to the Director, Clinical Operations, 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. Specifically, you will be responsible for: 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 Skills, Experience and Education: RN or bachelor’s degree in biological sciences or related health related field required. 1-3-years relevant experience in the pharmaceutical or biotech industry. 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 and people skills. Demonstrate proficiency in Microsoft Word, Excel, and PowerPoint. Demonstrated ability to multi-task, prioritize options. Travel may be required (~25%). Preferred Skills: Experience in working with cooperative group studies and investigator sponsored trials, preferred. Experience in clinical operations or clinical research. Experience of Global clinical trial operations outside the USA. Knowledge of the APAC region. #LI-Hybrid #LI-DN1 The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training. Please note that base pay salary range 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. Base Pay Salary Range $90,000—$108,000 USD We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message. Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address. If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

Responsibilities

The Clinical Trial Assistant will act as a central contact for clinical study teams, assisting with study document management, system maintenance, and trial master file upkeep. They will also coordinate cross-functional study activities, schedule meetings, and support site start-up and close-out processes.