Clinical Trial Manager (9-Month) - Rare Diseases & Oncology

CRISPR Therapeutics, Inc.; Boston (MA); On-site; USD 124,000 - 138,000; Full time

Job summary

CRISPR Therapeutics, Inc. in Boston is seeking an experienced Clinical Operations professional to lead trial management for rare diseases and oncology indications.

You will oversee CROs, ensure timelines, and guide study execution with cross‑functional teams. The role emphasizes hands-on site management, collaboration with KOLs, and adherence to ICH/GCP CFR standards, with travel up to 15–20% internationally and domestically.

Qualifications

• BS/BA/BSN in health/science with 7+ years in clinical research.
• 2+ years Clinical Trial Management experience.
• Excellent communication, writing and presentation skills.
• Willingness to travel domestically and internationally up to 15–20%.

Responsibilities

• Manage CROs/vendors for assigned trials ensuring adherence to scope and budget.
• Identify issues and implement solutions to ensure timelines are maintained.
• Develop and maintain tracking tools for clinical trials (site start-up, enrollment, visits, data entry, action items).
• Oversee maintenance of the eTMF and coordinate with finance for budgets.
• Plan and participate in advisory boards and investigator trainings.

Skills

Excellent communication

Cross-functional collaboration

Independent working

Travel readiness

Education

BS/BA/BSN – health/science

MS or advanced degree

Job description

CRISPR Therapeutics, Inc. in Boston is seeking an experienced Clinical Operations professional to lead trial management for rare diseases and oncology indications.

You will oversee CROs, ensure timelines, and guide study execution with cross‑functional teams. The role emphasizes hands-on site management, collaboration with KOLs, and adherence to ICH/GCP CFR standards, with travel up to 15–20% internationally and domestically.