Temp Director, Clinical Science at Revolution Medicines

Redwood City, California, United States -

Full Time

Start Date

Immediate

Expiry Date

26 Dec, 25

Salary

0.0

Posted On

27 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Science, Data Monitoring, Data Cleaning, Medical Monitoring, Safety Reviews, Data Analysis, Clinical Trials, Oncology, Interpersonal Skills, Communication Skills, Strategic Thinking, Regulatory Requirements, Biostatistics, Team Collaboration, Attention to Detail, Independent Decision Making

Industry

Hospitals and Health Care

Description

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 be an essential contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on protocol-specific activities. The Clinical Scientist will work on cross-functional study management teams and contribute to the design, planning, and implementation of study protocols for assigned investigational products. Importantly, the Clinical Scientist will help lead data cleaning and monitoring activities of assigned study protocols of behalf of the Clinical Science function. Responsible for data monitoring and cleaning of clinical/medical relevant data points Support senior team members with medical monitoring reports, safety reviews, and reviewing TFLs. May provide analytical support of clinical trial data (safety and efficacy), including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations. May analyze information to assess issues relating to protocol conduct and/or individual subject safety thru data review. Assist in communicating a clear overview of trial results. May provide organizational support for Data Monitoring Committees other applicable data review committees including preparing updates and data reviews. May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalations. Support the development of abstracts, posters, and content for scientific meetings, conferences and publications. May support preparations for investigator meetings and scientific conferences. Conduct literature reviews as needed. Required Skills, Experience and Education: At least 5+ years of experience at a pharmaceutical, CRO or biotechnology company as a Clinical Scientist. Applications failing to meet this specific requirement will not be considered. Master/PhD degree in health science field, PharmD, MD or non-US equivalent, or other relevant advanced degree in a health science field. Experience in oncology or oncology immunotherapy clinical trials preferred. Significant experience with electronic data capture databases (preferably RAVE), data analysis tools (eg, Spotfire) and data cleaning methodology. Preferred Skills: Ability to think strategically, innovatively, and tactically with an interest in clinical research and drug development. Demonstrated ability to evaluate, interpret and present complex scientific data (preclinical, clinical, translational) to inform scientific hypotheses and development strategy. Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies. Must be willing and possess the expertise to work effectively in a fast-paced, team-based matrix environment as well as the ability to function independently as appropriate. Flexible to accommodate changes in team and project needs. Ability to handle multiple projects at a time and have a strong attention to detail while understanding the higher-level strategy. Excellent interpersonal, verbal, and written communication skills. Ability to make independent, timely and appropriate decisions. 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 privacy@revmed.com. #LI-Hybrid #LI-AP1

Responsibilities

The Clinical Scientist will contribute to the scientific, clinical, and operational scope of clinical development programs, focusing on protocol-specific activities. Responsibilities include data monitoring, cleaning, and supporting senior team members with medical monitoring reports and safety reviews.