Temp Clinical Scientist, Clinical Development bei Revolution Medicines

Revolution Medicines 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 Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

The Clinical Scientist will contribute to the scientific, clinical, and operational scope of assigned study protocols. This role will work with the cross-functional teams for the design, execution, and monitoring of clinical studies, as well as assist with data review, interpretation, and communication to both internal stakeholders. Oncology and/or late-stage experience is preferred.  Contribute to clinical development strategy and execution of the Clinical Development Plan (CDP).

• Partner with cross-functional teams with oversight from senior team members to conduct clinical studies, including study start up, execution and close out activities, database set up, data review/analysis, and preparation of study reports.

• Contribute to the development of program-level documents, including but not limited to clinical protocols, investigator’s brochure, clinical study reports, abstracts and manuscripts, presentations, and various other internal and external documents and communications as needed.

• Conduct ongoing data reviews; prepare and present summaries to internal stakeholders.

• Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety.

• Interact with internal and external stakeholders (investigators, study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalation.

• Conduct literature reviews as needed.

• Travel: Up to 20%.

Required Skills, Experience and Education:

• BS/BA or master’s degree in a scientific discipline, or other relevant advanced degree in a health science field.

• Minimum 2 years of experience in the pharmaceutical or biotechnology industry as a clinical scientist or related role in oncology solid tumors.

• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.

• Detail-oriented with ability prioritize tasks and function independently as appropriate.

• Strong organizational skills and an ability to interpret, discuss, and report trial/program level data effectively and identify trends.

• Proficient with software tools (Microsoft Office), Electronic Data Capture, and other custom web-based software.

• Excellent written and verbal communication skills.

This is a contract position that will be employed through a third-party recruiting agency. The agency will provide the pay range, which will be based on several factors, including job-related skills, experience, market conditions, and relevant education or training.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes the protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact [email protected]. 

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