DMPK Study Coordinator – Cross-Functional Biotech Role

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

Job summary

Editas Medicine, a leader in genome editing, seeks a Study Coordinator to support nonclinical drug development at Cambridge, MA. You will manage timelines, documents, and sample logistics within the DMPK, Nonclinical Safety, and Translational Science teams.

You will coordinate data, ensure LIMS integrity, and partner with science and informatics to streamline workflows. This six-month contractor role offers exposure to multiple stages of drug development.

Qualifications

• BS with two years of biotech/pharma/CRO experience.
• Proficiency with Smartsheet and ThinkCell.
• Experience with sample tracking and shipping.
• Experience with LIMS such as Benchling.
• Excellent cross-functional communication.
• Ability to work in a dynamic, multidisciplinary environment.

Responsibilities

• Timeline & Progress Management: Build, track and manage nonclinical timelines to meet milestones.
• Information & Document Control: Keep study documents organized and accessible to authors and scientists.
• Sample Logistics: Coordinate end-to-end flow, shipment and receipt of samples across groups.
• LIMS Data Integrity & Innovation: Enter data into LIMS and work with Informatics to improve templates.
• Data Organization: Synthesize data to support study leads in presentations and reports.
• Cross-Functional Communication: Keep internal/external contributors informed on timelines and data.

Skills

Project management

Sample tracking

LIMS (Benchling)

Cross-functional comms

Multi-tasking

Tools

Smartsheet

ThinkCell

GraphPad Prism

Job description

Editas Medicine, a leader in genome editing, seeks a Study Coordinator to support nonclinical drug development at Cambridge, MA. You will manage timelines, documents, and sample logistics within the DMPK, Nonclinical Safety, and Translational Science teams.

You will coordinate data, ensure LIMS integrity, and partner with science and informatics to streamline workflows. This six-month contractor role offers exposure to multiple stages of drug development.