Global Clinical Data Management Director

Korrobio; Cambridge (MA); On-site; USD 170,000 - 230,000; Full time

Benefits offered by this job

Equity-based compensation

Medical, dental, vision coverage

401(k) retirement plan

Life insurance

Free parking

Job summary

Korro seeks an Associate Director, Clinical Data Management to lead data management across global studies, ensuring audit-ready data for regulatory submissions. You will oversee CROs, database builds, data cleaning, and data transfer specifications, aligning with study milestones and budgets.

The role requires deep regulatory knowledge, strong communication, and the ability to drive data quality in a fast-paced environment. On-site in Cambridge, MA with global collaboration.

Qualifications

• Bachelor’s degree in Life Sciences, Computer Science, or related field; advanced degree preferred.
• Minimum 8 years in clinical data management/clinical trials across Phases I–IV.
• Experience managing CRO relationships and overseeing outsourced CDM activities.
• Proficient in EDC platforms, data cleaning, queries, and database lock processes.

Responsibilities

• Lead data management activities across global studies/programs from start-up to database lock.
• Oversee CRO/vendor performance and data management deliverables to ensure timelines.
• Provide input on protocols, SAPs, data flows, and data specifications.
• Ensure compliance with regulatory guidance (FDA/ICH/CDISC) and SOPs.
• Coordinate data metrics, listings, and audits with cross-functional teams.

Skills

Regulatory knowledge

Data management

EDC platforms

Vendor management

Cross-functional collaboration

Education

Bachelor's degree

Advanced degree preferred

Tools

Medidata Rave

Veeva Vault EDC

CDISC standards

Job description

Korro seeks an Associate Director, Clinical Data Management to lead data management across global studies, ensuring audit-ready data for regulatory submissions. You will oversee CROs, database builds, data cleaning, and data transfer specifications, aligning with study milestones and budgets.

The role requires deep regulatory knowledge, strong communication, and the ability to drive data quality in a fast-paced environment. On-site in Cambridge, MA with global collaboration.