Clinical Research Nurse Coordinator (Per Diem)

UMass Med School; Worcester (MA); On-site; USD 47,000 - 73,000; Part time

Job summary

University of Massachusetts Medical School in Worcester, MA seeks a Research Nurse Coordinator at open ranks for per diem assignments. The role supports complex protocol testing, investigational drugs and devices, and serves as a liaison to PMs, IRB, and sponsors to ensure GCP throughout the study life cycle.

Responsibilities include screening, randomization, enrollment, consent, regulatory documentation, adverse event reporting, and coordination of procedures with investigators and sponsoring

Qualifications

• RN with current registration to practice nursing in Massachusetts.
• 3-5 years of relevant nursing experience.
• Proficiency in electronic medical records and relevant computer software.
• Strong oral and written communication skills; attention to detail is essential.
• Ability to travel to off-site locations.
• Bachelor's degree in Nursing (preferred).
• Experience with OnCore and Epic (preferred).
• Phlebotomy and EKG skills (preferred).
• BLS Certification (preferred).

Responsibilities

• Review and abstract medical record information per protocol and HIPAA requirements.
• Ensure proper adherence to randomization, study drug dosing and administration per protocol.
• Screen patients, randomize, enroll, and consent in accordance with GCP standards.
• Maintain regulatory documents and report findings to PI, sponsor, and IRB as needed.
• Coordinate study procedures and data entry in the clinical trial management system.

Skills

RN license

Clinical research experience

EMR proficiency

Communication skills

Travel ability

Education

Bachelor's degree in Nursing

Tools

OnCore

Epic

Job description

University of Massachusetts Medical School in Worcester, MA seeks a Research Nurse Coordinator at open ranks for per diem assignments. The role supports complex protocol testing, investigational drugs and devices, and serves as a liaison to PMs, IRB, and sponsors to ensure GCP throughout the study life cycle.

Responsibilities include screening, randomization, enrollment, consent, regulatory documentation, adverse event reporting, and coordination of procedures with investigators and sponsoring