Associate Director, Global Clinical Data Management

Scorpion Therapeutics; Cambridge (MA); On-site; USD 140,000 - 200,000; Full time

Job summary

Scorpion Therapeutics is seeking an Associate Director of Clinical Data Management to lead global data activities across early- and late-phase trials in genetic medicine. You will oversee end-to-end data management, from study start-up through database lock, and ensure regulatory compliance (GxP, 21 CFR Part 11, ICH, GCDMP).

You will collaborate with Clinical Development, Biostatistics, Regulatory, and Operations to maintain data quality, integrity, and audit readiness for regulatory submissions.

Qualifications

• 8+ years in clinical data management and CRO oversight.
• Experience with Phase I–IV outsourced trials.
• Strong communication and leadership in a fast-paced environment.

Responsibilities

• Oversee end-to-end data management from start-up to database lock.
• Collaborate with Clinical Development, Biostatistics, Regulatory, and Operations to ensure data quality and audit readiness.
• Manage data system configurations, transfer protocols, validation activities, and data quality metrics.

Skills

Cross-functional leadership

Regulatory compliance

Data quality management

Education

Bachelor's in Life Sciences

Tools

Medidata Rave

CDISC standards

RBM

Job description

Scorpion Therapeutics is seeking an Associate Director of Clinical Data Management to lead global data activities across early- and late-phase trials in genetic medicine. You will oversee end-to-end data management, from study start-up through database lock, and ensure regulatory compliance (GxP, 21 CFR Part 11, ICH, GCDMP).

You will collaborate with Clinical Development, Biostatistics, Regulatory, and Operations to maintain data quality, integrity, and audit readiness for regulatory submissions.