Associate Director, Clinical Data Management - Data Integrity Lead

Gavroche; Cambridge (MA); On-site; USD 147,000 - 210,000; Full time

Job summary

Relay Therapeutics in Cambridge, MA, is seeking an Associate Director of Clinical Data Management to lead data integrity and quality across studies. You will oversee CROs, drive database development and CRF design, and ensure compliance with global regulations.

The role requires extensive data management experience and strong collaboration across a fast-paced, science-driven team. The candidate will guide data standards, SOP development, and training while managing multiple studies from design

Qualifications

• 7+ years in pharmaceutical/biotechnology as a Data Manager (sponsor experience preferred).
• Experience with data collection and cleaning across Phase I–III. Oncology exposure preferred.
• Strong knowledge of global regulatory requirements (US CFR, EU CTD, ICH GCP, CDISC).
• Experience overseeing CROs/vendors and data management metrics.

Responsibilities

• Oversee data management activities for assigned studies, including timelines and deliverables.
• Lead database development and eCRF design, UAT, data import specs, CRF completion guidelines, and data operation manuals.
• Lead data validation specifications and programs to ensure data accuracy (edit checks, DMP).
• Manage data cleaning through to database lock; handle queries, listings, SAE reconciliation, coding, and lab data integration.
• Collaborate with cross-functional Relay teams to ensure timely, high-quality data deliverables.
• Ensure compliance with global regulatory standards and participate in data standards initiatives and SOP development.

Skills

Data management

CRO oversight

Regulatory compliance

Study data handling (Phase I-III)

Oncology domain knowledge

Communication skills

Public speaking

Project management

Tools

eCRF design

DMP development

Job description

Relay Therapeutics in Cambridge, MA, is seeking an Associate Director of Clinical Data Management to lead data integrity and quality across studies. You will oversee CROs, drive database development and CRF design, and ensure compliance with global regulations.

The role requires extensive data management experience and strong collaboration across a fast-paced, science-driven team. The candidate will guide data standards, SOP development, and training while managing multiple studies from design