Clinical Trial Assistant

Revolution Medicines•Redwood City, CA

6d•Hybrid

About The Position

Revolution Medicines is a global, commercial-stage 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. 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.

Requirements

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.

Nice To Haves

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.

Responsibilities

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.