Wellnet Research Solutions is seeking a Clinical Research Coordinator (CRC) to support Rheumatology clinical trials. This is an on-site role working closely with the Principal Investigator (PI) to coordinate and execute daily study activities in a fast-paced clinical research environment.
In this position, you will be responsible for coordinating patient visits, supporting recruitment and follow-ups, maintaining accurate study documentation, and ensuring compliance with study protocols and regulatory requirements. You will also collaborate with investigators, sponsors, and internal teams to ensure smooth study execution.
We are seeking candidates with prior clinical research experience who are comfortable working in a structured and detail-oriented environment. Experience in dermatology is strongly preferred; however, candidates with relevant clinical trial experience in other therapeutic areas will be considered. Bilingual (English/Spanish) skills are preferred but not required.
This role is best suited for candidates who have previously worked in clinical trial settings and understand study workflows, patient coordination, and regulatory documentation.
Candidates should be reasonably located near Plantation, FL (approximately within 15–20 miles), as this is an on-site position.
Application Requirement:
To be considered, please include a brief summary (2–3 sentences) describing your clinical research experience and therapeutic areas you have worked in. Applications without this information may not be reviewed.
Note:
Only candidates with relevant clinical research experience will be contacted.
Benefits:
- Paid time off
Experience:
-Rheumatology: 1 year
-License/Certification:
GCP (Required)
IATA Certification (Required)
-Work Location: In person
Wellnet Research Solutions is a multidisciplinary site network managing and supporting multiple affiliated research sites across the United States. We are committed to delivering high-quality clinical research services through a highly trained, experienced, and dedicated team of professionals. Our network prioritizes ethical and safe medical care for study participants while providing sponsors and CROs with reliable, high-quality clinical data in strict compliance with Good Clinical Practice (GCP) guidelines and applicable regulatory standards.