Clinical Trial Assistant

Clinical Trial Assistant

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

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.

Base Pay Salary Range

$90,000 - $108,000 USD