Clinical Trial Assistant

Revolution Medicines•Redwood City, CA

4h•Onsite

About The Position

Revolution Medicines is a late-stage clinical oncology company focused on developing novel targeted therapies for patients with RAS-addicted cancers. Their R&D pipeline includes several RAS(ON) inhibitors currently in clinical development. As a Clinical Trial Assistant in Clinical Operations, this entry-level professional will serve as a central contact for clinical study teams, assisting with the clinical execution and management of RevMed clinical trials. The role initially reports to the Director, Clinical Operations.

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.
Travel may be required (~25%).

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.