Lead, Clinical Data Management & Data Quality

Relay Therapeutics, Inc.; Cambridge (MA); On-site; USD 129,000 - 184,000; Full time

Job summary

Relay Therapeutics, Inc. is seeking a Senior Manager, Clinical Data Management to lead data management across clinical studies and ensure data integrity from collection through database lock.

You will oversee CROs, design eCRFs, and drive data validation and quality controls in a fast-paced biotech environment. You will collaborate with cross-functional teams, manage timelines, and ensure regulatory compliance, with a focus on Oncology studies and Medidata Rave familiarity.

Qualifications

• 7+ years of experience in pharma/biotech/CRO as a Data Manager
• Experience with oncology data cleaning is a plus
• Familiarity with Medidata Rave and EDC systems

Responsibilities

• Oversee data management activities for assigned studies, including timelines and deliverables
• Oversee CROs and vendors for outsourced data management and monitor performance
• Lead database development and eCRF design, UAT, data import specs, CRF completion guidelines, and related operations manuals
• Lead data validation specifications to ensure accuracy of trial data
• Execute or oversee data cleaning through to database lock, including queries and listings
• Provide technical and business DM expertise in support of data management deliverables
• Collaborate with study team members and CROs on data cleaning and database lock activities
• Review and QC study eTMF documentation for Data Management
• Oversee RAVE user access QCs
• Represent DM in study team meetings and ensure regulatory compliance

Skills

Data management

CRO/vendor oversight

Data cleaning

eCRF design

Data validation

Communication

Tools

Medidata Rave

Advanced Excel

Job description

Relay Therapeutics, Inc. is seeking a Senior Manager, Clinical Data Management to lead data management across clinical studies and ensure data integrity from collection through database lock.

You will oversee CROs, design eCRFs, and drive data validation and quality controls in a fast-paced biotech environment. You will collaborate with cross-functional teams, manage timelines, and ensure regulatory compliance, with a focus on Oncology studies and Medidata Rave familiarity.