Clinical Research Coordinator — Onsite with Strong Benefits

knownwell; Woburn (MA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401K retirement plan with companymatch

Up to 20 days PTO + holidays

Up to 14 weeks parental leave

Annual WFH stipend

Job summary

knownwell, Inc. is seeking a Clinical Research Coordinator in Woburn, MA to oversee all aspects of clinical trials. The role requires coordinating patient recruitment, visits, data management, and regulatory compliance, with on-site duties primarily 4-5 days per week.

The candidate should have clinical research experience, GCP familiarity, and strong organizational and communication skills to support sponsor expectations and IRB submissions.

Qualifications

• Bachelor's degree in life sciences, nursing or healthcare field.
• CCRC Certification and/or master’s degree preferred.
• Solid understanding of GCP, FDA guidelines and regulatory requirements.

Responsibilities

• Coordinate and manage all aspects of clinical trials, including patient recruitment, screening and enrollment.
• Oversee visits, data/sample collection, site initiation, monitoring, and regulatory compliance.
• Maintain study documentation, report adverse events, and manage drug/sample handling.

Skills

Phlebotomy

Leadership

Time management

Communication

Education

Bachelor's degree in life sciences/healthcare

CCRC Certification

Master’s degree preferred

Tools

CTMS

EDC

Regulatory databases

Job description

knownwell, Inc. is seeking a Clinical Research Coordinator in Woburn, MA to oversee all aspects of clinical trials. The role requires coordinating patient recruitment, visits, data management, and regulatory compliance, with on-site duties primarily 4-5 days per week.

The candidate should have clinical research experience, GCP familiarity, and strong organizational and communication skills to support sponsor expectations and IRB submissions.