Coordinate all aspects of assigned clinical studies related to advanced wound care and skin substitute therapies
Screen, recruit, and consent eligible patients in accordance with study protocols
Schedule and conduct study visits; perform clinical assessments within RN scope of practice
Ensure thorough, accurate documentation of wound characteristics and treatment response
Monitor patient safety and report adverse events in line with regulatory standards
Maintain compliance with FDA, IRB, GCP, and sponsor requirements
Prepare and update regulatory binders and essential trial documents
Enter and track accurate study data in electronic data capture (EDC) systems
Serve as the primary liaison between investigators, sponsors, CROs, and clinical teams
Provide regular study updates to leadership and participate in training/initiation sessions
Uphold the highest level of professionalism, confidentiality, and integrity in all work

Requirements

Possess an active Registered Nurse (RN) license in good standing
Have experience coordinating or supporting clinical trials
Demonstrate strong knowledge of clinical research processes and regulatory standards (GCP)
Are highly detail-oriented, organized, and have excellent written/verbal communication skills
Are adept with data entry and electronic data capture systems
Can manage multiple studies and timelines independently while contributing to a collaborative team

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical assessmentsdata entryelectronic data capture (EDC) systemsclinical trial coordinationwound careskin substitute therapies

Soft Skills

detail-orientedorganizedwritten communicationverbal communicationcollaborative

Certifications

Registered Nurse (RN) license