Manager, Clinical Data Management

CRISPR Therapeutics AG

Base: $123,000 to $133,000; bonus/equity: included...
Fully remote
7+ years clinical data management experience
Medidata rave edc database proficiency
Cdash/sdtm/cdisc standards knowledge
CRISPR Therapeutics AG is seeking a Manager of Clinical Data Management to lead clinical data management activities for their gene editing programs. The ideal candidate will have extensive experience in clinical data management within a regulatory environment and will be responsible for ensuring high-quality data capture and vendor oversight

Job Summary

  • The Manager of Clinical Data Management will lead clinical data management activities across all stages of clinical development for CRISPR Therapeutics.
  • This role serves as the primary liaison with CROs and third-party vendors while overseeing database design and UAT cycles to ensure high-quality data.
  • CRISPR Therapeutics fosters a dynamic workplace balancing remote flexibility with at least three days of in-person collaboration per week.

Matching Summary

Match Score: 85

CRISPR Therapeutics AG is seeking a Manager of Clinical Data Management to lead clinical data management activities for their gene editing programs. The ideal candidate will have extensive experience in clinical data management within a regulatory environment and will be responsible for ensuring high-quality data capture and vendor oversight.

Salary

Base: $123,000 to $133,000; Bonus/Equity: Included; Benefits: Not specified

Skills & Requirements

Must-have

  • 7+ years clinical data management experience
  • Medidata Rave EDC database proficiency
  • CDASH/SDTM/CDISC standards knowledge
  • Medical coding with MedDRA and WHO
  • GCP ICH FDA regulatory compliance

Nice-to-have

  • Experience in small biotech environment
  • J-Review or Business Objects reporting
  • Entrepreneurial spirit and proactive ownership
  • Ability to manage shifting priorities
  • Strong analytical problem-solving skills

Key Requirements

  • Bachelor's degree required; Master's preferred
  • Minimum 7 years progressive experience in regulatory environment
  • Working knowledge of medical terminology and coding dictionaries

Work Rights

Not specified

Tailored Resume

Cover Letter