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Clinical Trial Assistant - Contractor

Redwood City, CA 94063

Posted: 02/22/2024 Employment Type: Contract Job Category: Clinical Development and Operations Job Number: 599467 Is job remote?: No Country: United States

Job Description

  Clinical Trial Assistant/Associate - Contractor
Our client is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding scientists 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. As the Senior Clinical Trial Assistant of Clinical Operations, initially reporting to the Associate Director/Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support 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 Experience, Skills, and Education:

  • RN or bachelor’s degree in biological sciences or related health related field required.

  • Minimum of 3-years relevant experience in the pharmaceutical or biotech industry, preferably in clinical operations or clinical research-related experience.

  • 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 interpersonal skills.

  • Demonstrate proficiency in Microsoft Word, Excel and PowerPoint.

  • Demonstrated ability to multi-task, prioritize options.

  • Travel may be required (~25%).
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