Clinical Research Coordinator RN

Green Life Science; Philadelphia (Philadelphia County); On-site; USD 60,000 - 90,000; Full time

Job summary

Green Life Science is seeking a Clinical Research Coordinator (CRC) with an active RN license to join our Philadelphia team. This hands-on, participant-facing role combines nursing expertise with clinical trial coordination to ensure participant safety, accurate documentation, and protocol compliance.

You will conduct visits, assess participants, perform required procedures, and maintain source documentation while coordinating with investigators, sponsors, and monitors.

Qualifications

• Active RN license is required.
• Previous clinical research or trial experience preferred.
• Strong hands-on patient assessment and clinical care skills.
• Experience with vital signs, ECGs/EKGs and phlebotomy.
• Knowledge of clinical documentation, patient safety and research protocols.

Responsibilities

• Coordinate trials from screening to completion.
• Conduct study visits, patient assessments and protocol procedures.
• Review medical histories and assess eligibility.
• Obtain informed consent per protocol and regulatory requirements.
• Perform vital signs, ECGs and blood collection as required.
• Monitor participant safety and document adverse events.

Skills

Patient assessment

Clinical care

Communication

Attention to detail

On-site work Philadelphia

Education

RN license

Tools

EDC systems

Source documentation systems

Job description

An established clinical research organisation is seeking a Clinical Research Coordinator (CRC) with an active Registered Nurse (RN) licence to join its Philadelphia team.

This is a hands-on, participant-facing role supporting the coordination and delivery of clinical trials across a range of therapeutic areas. The successful candidate will combine nursing expertise with clinical research coordination, ensuring participant safety, accurate documentation and compliance with study protocols.

Key Responsibilities

• Coordinate clinical trials from participant screening and enrolment through study completion.
• Conduct study visits, patient assessments and protocol-specific clinical procedures.
• Review medical histories and assess participants against study eligibility criteria.
• Obtain informed consent in accordance with approved protocols and regulatory requirements.
• Perform vital signs, 12-lead ECGs/EKGs, phlebotomy and specimen collection as required.
• Monitor participant safety and document adverse events, escalating concerns appropriately.
• Maintain accurate source documentation, study records and electronic data capture (EDC) systems.
• Support participant recruitment, retention and follow-up throughout the study lifecycle.
• Ensure compliance with study protocols, ICH-GCP, FDA regulations and site SOPs.
• Coordinate with Principal Investigators, Sub-Investigators, sponsors, CROs and study monitors.
• Assist with monitoring visits, audits, data queries and regulatory documentation.
• Support the safe handling, processing and shipment of biological specimens in accordance with study requirements.

Requirements

• Active Registered Nurse (RN) licence.
• Previous clinical research or clinical trial experience preferred.
• Strong hands-on patient assessment and clinical care skills.
• Experience with vital signs, ECGs/EKGs and phlebotomy.
• Knowledge of clinical documentation, patient safety and research protocols.
• Strong organisational skills and attention to detail.
• Excellent communication and participant-facing skills.
• Ability to work on-site in Philadelphia, PA.

Preferred Qualifications

• Experience supporting Phase I-IV clinical trials.
• Background in vaccine, cardiology, metabolic, diabetes, obesity or other interventional studies.
• Familiarity with EDC systems, source documentation and regulatory requirements.
• Experience working within a dedicated clinical research site.

Why Consider This Opportunity?

• Combine nursing expertise with hands-on clinical research.
• Work directly with participants throughout the clinical trial process.
• Gain exposure to multiple therapeutic areas.
• Contribute to the development of new treatments and the advancement of medical research.