Description

You will manage clinical research activities under the direction of the Principal Investigator, coordinating protocols, collecting data, recruiting and screening participants, and maintaining study files. Your work ensures regulatory compliance and supports high-quality clinical trials.

Requirements

• Experience as Clinical Research Coordinator
• Knowledge of FDA CFR, GCP, and company SOPs
• Ability to manage multiple protocols and meet recruitment goals
• Strong organizational and communication skills
• Phlebotomy and basic lab test skills (preferred)

Responsibilities

• Manage conduct of clinical research activities under direction of PI
• Coordinate protocol implementation, patient assessments, scheduling, and study file maintenance
• Recruit and screen potential participants through chart review and referral follow-up
• Record data in clinical trial management system and maintain source documentation
• Perform study tasks: informed consent, phlebotomy, vital signs, ECG, and drug administration