Clinical Operations Assistant — Entry-Level Trials

Revolution Medicines; San Francisco (CA); On-site; USD 90,000 - 108,000; Full time

Job summary

Revolution Medicines, based in Redwood City, CA, is seeking an entry-level Clinical Trial Assistant reporting to the Director of Clinical Operations to support clinical trial execution and management.

You will assist in the development and archiving of study documents, maintain TMF and clinical systems, and coordinate meetings, site information, and cross-functional activities with CROs and vendors. Travel (~25%) may be required.

Qualifications

• RN or bachelor’s degree required in biological sciences or related health field.
• 1-3 years of experience in pharmaceutical or biotech industry.
• Thrives in collaborative team setting with willingness to deploy innovative approaches.
• Excellent written and verbal communication and people skills.
• Proficient in Microsoft Word, Excel and PowerPoint.
• Travel may be required (~25%).

Responsibilities

• Assisting in development, review, distributing and archiving of study documents and reports.
• Assisting with updating and maintaining clinical systems and reporting tools.
• Set up and maintenance of the TMF or coordinate with CRO to audit discrepancies.
• Create, maintain and track information for key study activities.
• Assist in meeting materials, scheduling, agendas and minutes for internal team meetings.
• Gather investigator and site information to support start-up, maintenance and close-out.
• Coordinate with cross-functional study teams and vendors for trial activities.
• Support other clinical operations activities as appropriate.

Skills

Collaborative team player

Multi-tasking

Prioritization

Travel readiness

Education

RN or biology-related bachelor’s degree

Tools

Word

Excel

PowerPoint

Job description

Revolution Medicines, based in Redwood City, CA, is seeking an entry-level Clinical Trial Assistant reporting to the Director of Clinical Operations to support clinical trial execution and management.

You will assist in the development and archiving of study documents, maintain TMF and clinical systems, and coordinate meetings, site information, and cross-functional activities with CROs and vendors. Travel (~25%) may be required.