Contractor: Nonclinical Study Coordinator (DMPK)

Editas Medicine; Cambridge (MA); On-site; USD 55,000 - 62,000; Part time

Job summary

Editas Medicine is seeking a Non-clinical Study Coordinator to join the DMPK, Nonclinical Safety, and Translational Science Team. This 6 month contractor role will track timelines, samples, and data across functional groups to support regulatory submission.

You will manage nonclinical timelines, document control, and cross-functional communication, ensuring data integrity in LIMS and rapid information flow to study leads.

Qualifications

• BS with two years of biotech/pharma/CRO experience supporting nonclinical or translational studies.
• Proficiency with project management tools (Smartsheet, ThinkCell).
• Experience with sample tracking and shipping; familiarity with LIMS (Benchling).

Responsibilities

• Coordinate timelines and deliverables to keep nonclinical programs on target.
• Maintain meticulous study documents and ensure accessible reports.
• Coordinate end-to-end sample logistics across teams.
• Ensure LIMS data integrity and collaborate with informatics for templates.
• Organize study data to support leads during presentations and reports.
• Act as a communications hub for timeline shifts, sample status, and data.

Skills

Project management

Cross-functional communication

Data organization

Education

BS in biotech/pharma or related field

Tools

Smartsheet

ThinkCell

Benchling

Job description

Editas Medicine is seeking a Non-clinical Study Coordinator to join the DMPK, Nonclinical Safety, and Translational Science Team. This 6 month contractor role will track timelines, samples, and data across functional groups to support regulatory submission.

You will manage nonclinical timelines, document control, and cross-functional communication, ensuring data integrity in LIMS and rapid information flow to study leads.