Intern, External Data Coordinator

Revolution Medicines • Redwood City, CA

22h • Hybrid

About The Position

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:
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.

What This Job Offers

• Career Level: Intern