Per Diem Research Nurse Coordinator (Clinical Trials)

UMass Med School; Worcester (MA); On-site; USD 55,104 - 82,656; Full time

Job summary

The University of Massachusetts Medical School in Worcester is seeking a Research Nurse Coordinator (Open Rank) to manage complex protocol tasks, coordinate care, and ensure GCP compliance across study life cycles. You will liaise with investigators, sponsors, IRB, and clinical partners to uphold protocol integrity and patient safety.

Responsibilities include screening, enrolling, consenting participants, coordinating study procedures, maintaining regulatory documents, and contributing to QA and

Qualifications

• RN with current Massachusetts license.
• 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.
• Ability to work in a team environment and travel to off-site locations.

Responsibilities

• Review and abstract medical record information per protocol, HIPAA, and regulatory requirements.
• Coordinate randomization, dosing, and administration with investigational pharmacy.
• Participate in quality assurance audits and screen/enroll/consent participants per GCP.
• Maintain patient confidentiality and regulatory documentation across the study life cycle.
• Record study events and protocol procedures; identify and report adverse events as required.
• Coordinate all study procedures and ensure data entry into the trial management system.

Skills

Massachusetts RN license

Nursing experience 3-5 years

EMR proficiency

Strong communication

Teamwork

Travel ability

Education

Bachelor's degree in Nursing

Tools

OnCore

Epic

Job description

The University of Massachusetts Medical School in Worcester is seeking a Research Nurse Coordinator (Open Rank) to manage complex protocol tasks, coordinate care, and ensure GCP compliance across study life cycles. You will liaise with investigators, sponsors, IRB, and clinical partners to uphold protocol integrity and patient safety.

Responsibilities include screening, enrolling, consenting participants, coordinating study procedures, maintaining regulatory documents, and contributing to QA and