Description

Our client, a well-established dermatology practice known for clinical excellence, is hiring a Clinical Research Coordinator. This role offers an excellent opportunity to contribute to innovative dermatologic therapies within a collaborative, patient-focused environment. The successful candidate will coordinate and manage dermatology clinical trials, ensuring compliance with regulatory standards while supporting study participants and maintaining meticulous documentation.

Responsibilities:

• Screen, recruit, and enroll participants for dermatology clinical trials
• Conduct informed consent discussions with study participants
• Coordinate and perform study visits according to protocol requirements
• Maintain accurate source documentation and Case Report Forms (CRFs)
• Ensure compliance with FDA, GCP, and IRB regulations
• Manage investigational product accountability and study materials
• Document and report adverse events (AEs) and serious adverse events (SAEs)
• Maintain regulatory files including Trial Master Files (TMF)
• Assist physicians with dermatologic study procedures
• Obtain standardized pre- and post-treatment clinical photography
• Communicate effectively with sponsors, monitors, and internal research staff throughout the study
• Occasional travel for sponsor training may be required

Requirements

Requirements:

• Prior experience as a Clinical Research Coordinator or research assistant; dermatology research experience strongly preferred
• Knowledge of Good Clinical Practice (GCP) and FDA regulations
• Understanding of clinical trial processes and medical terminology
• Familiarity with HIPAA and research compliance standards
• Strong organizational and documentation skills
• Ability to manage multiple studies and deadlines simultaneously
• Excellent interpersonal and communication skills
• Professional demeanor when interacting with patients, physicians, and sponsors
• Ability to work both independently and as part of a team
• CPR certification preferred