Intern, External Data Coordinator
About The Position
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: Support the external data activities related to clinical trials to ensure quality, on-time data management deliverables. Assist with the external data reconciliation of the clinical database against safety data, laboratory data and other third-party data as appropriate. Participate in the review of the clinical trial data in accordance with Data Management Plans (DMP), Edit Check Specifications and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete or implausible data. Collaborate cross-functionally with Clinical Operation, Clinical Development and other teams to support in the data review and query management to ensure that quality standards are achieved. Gain hands-on experience in a regulated biotech/pharmaceutical environment while developing a foundational understanding of the external data systems.
Requirements
- Currently pursuing a bachelor’s degree in Life Sciences, Computer Sciences or a related field.
- Strong attention to detail with the ability to follow written procedures.
- Basic understanding of clinical data management principles or regulated environments (academic coursework acceptable).
- Proficiency with Microsoft Office (Word, Excel, PowerPoint).
- Strong written and verbal communication skills.
- Ability to work independently as well as collaboratively in a team environment.
Nice To Haves
- Good oral and written communication skills.
- Demonstrate ability to work in a team environment and independently.
- Demonstrate good organizational ability and people skills.
Responsibilities
- Support the external data activities related to clinical trials to ensure quality, on-time data management deliverables.
- Assist with the external data reconciliation of the clinical database against safety data, laboratory data and other third-party data as appropriate.
- Participate in the review of the clinical trial data in accordance with Data Management Plans (DMP), Edit Check Specifications and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete or implausible data.
- Collaborate cross-functionally with Clinical Operation, Clinical Development and other teams to support in the data review and query management to ensure that quality standards are achieved.
- Gain hands-on experience in a regulated biotech/pharmaceutical environment while developing a foundational understanding of the external data systems.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Career Level
Intern
Number of Employees
251-500 employees
