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Clinical Scientist
| Company | Revolution Medicines |
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| Location | San Carlos, CA, USA |
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| Salary | $115000 – $144000 |
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| Type | Full-Time |
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| Degrees | Bachelor’s, Master’s |
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| Experience Level | Junior, Mid Level |
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Requirements
- 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.
- Proficient with software tools (Microsoft Office), Electronic Data Capture, and other custom web-based software.
- Excellent written and verbal communication skills.
- Detail-oriented with ability to 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.
- Has demonstrated adaptability and flexibility.
Responsibilities
- Contribute to the scientific, clinical, and operational scope of assigned study protocols.
- Work with cross-functional teams for the design, execution, and monitoring of clinical studies.
- Assist with data review, interpretation, and communication to both internal stakeholders.
- Contribute to clinical development strategy and execution of the Clinical Development Plan (CDP).
- Partner with cross-functional teams to conduct clinical studies, including study start up, execution and close out activities, database set up, data review/analysis, and preparation of study reports.
- Assist with study vendor selection and education.
- 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.
Preferred Qualifications
- Oncology and/or late-stage experience is preferred.
