Clinical Trial Assistant at Revolution Medicines

**Who this is for** This role is for an entry-level Clinical Operations Professional looking to contribute to late-stage clinical oncology trials. It's ideal fo

Work type: hybrid

Location: Redwood City, California, United States

Salary: $90,000 – $108,000/yr

Type: Full-time

Summary

**Who this is for** This role is for an entry-level Clinical Operations Professional looking to contribute to late-stage clinical oncology trials. It's ideal for someone driven to deploy innovative approaches in a high-energy, collaborative environment. **Key highlights** You will be a central contact for clinical study teams, assisting with the execution and management of clinical trials. This includes document management, updating clinical systems, TMF maintenance, and coordinating with cross-functional teams and vendors. **You might be a good fit if you...** - Have an RN or Bachelor's degree in biological sciences or a related health field. - Possess 1-3 years of relevant experience in the pharmaceutical or biotech industry. - Are proficient in Microsoft Word, Excel, and PowerPoint, with the ability to multi-task and prioritize. - Have excellent written and verbal communication and interpersonal skills.

Job 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.

• 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%).

• 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.

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.

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