Senior Clinical Scientist
Clinical Development
Posted on 3/28/2024
INACTIVE
Revolution Medicines

201-500 employees

Develops targeted therapies for RAS-addicted cancers.
Company Overview
REVOLUTION Medicines stands out in the oncology field for its unique approach to drug discovery, leveraging insights from nature and evolution to develop targeted therapies for RAS-addicted cancers. The company's robust drug discovery and medicinal chemistry capabilities have resulted in a deep pipeline of RAS inhibitors, with their most advanced product, RMC-4630, currently in a multi-cohort Phase 1/2 clinical program. This focus on genetic drivers and adaptive resistance mechanisms in cancer, coupled with their commitment to exploring mechanism-based dosing paradigms and in-pathway combinations, positions REVOLUTION Medicines as a leader in precision oncology.
Biotechnology

Company Stage

N/A

Total Funding

$1.3B

Founded

2014

Headquarters

Redwood City, California

Growth & Insights
Headcount

6 month growth

19%

1 year growth

54%

2 year growth

92%
Locations
San Carlos, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
CategoriesNew
Medical, Clinical & Veterinary
Diagnostics & Laboratory Professionals
Physicians & Surgeons
Requirements
  • BS/BA or master's degree in a scientific discipline, or other relevant advanced degree in a health science field.
  • Minimum 4 years of experience in the pharmaceutical or biotechnology industry as a clinical scientist or related role.
  • Experience supporting oncology clinical trials.
  • Strong experience with clinical data review and data quality assurance.
  • Knowledge and experience with clinical trial management and oversight.
  • Understanding and experience in clinical trial protocol and regulatory document authoring.
Responsibilities
  • Contribute to clinical development strategy and execution of the Clinical Development Plan (CDP) with a focus on early-phase development.
  • Partner with cross-functional teams with oversight from senior team members to conduct clinical studies, including study start up, execution and close out activities, 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 and external 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.