Clinical Research Coordinator (Adult & Pediatric) Full-Time | Onsite Compensation & Benefits $25•30/hour , based on experience and qualifications Full-time opportunity No evenings, weekends, or on-call responsibilities Employer-sponsored training for: CCMA (if not already certified) Phlebotomy BLS Good Clinical Practice (GCP) IATA Supportive, collaborative work environment with opportunities for professional growth

Schedule Monday-Thursday :

7:30 AM•4:30

PM Friday:

7:30 AM•12:30 PM Full-time only Limited travel to nearby locations may occasionally be required Key Responsibilities Coordinate and manage Phase II-IV clinical trials Screen and enroll eligible study participants Conduct informed consent discussions Review medical records and verify eligibility criteria Ensure strict protocol compliance and accurate documentation Maintain complete regulatory and study documentation Perform clinical procedures including blood draws, specimen processing, and vaccine administration (training available) Maintain investigational product accountability Coordinate protocol-required laboratory testing, medications, and follow-up visits Report adverse events within required timelines Communicate effectively with investigators, sponsors, monitors, and study participants Participate in sponsor visits and site meetings Assist with study start-up, participant recruitment, and retention efforts Mentor and assist with training new research staff when needed Preferred Therapeutic Experience Experience supporting studies in one or more of the following areas is highly preferred: Vaccines Weight Management Cardiovascular Health Dermatology Pediatric Clinical Research (for pediatric-focused opening) Qualifications Required Minimum 1 year of Clinical Research Coordinator experience (required) Minimum 1 year of direct patient care experience Experience coordinating Phase II-IV clinical trials Strong understanding of GCP and clinical research regulations Knowledge of medical terminology Excellent documentation and organizational skills Strong communication and interpersonal abilities Ability to manage multiple studies simultaneously Preferred CCMA certification (or willingness to obtain after hire) Blood draw/phlebotomy experience BLS certification GCP training/certification IATA certification Pediatric research experience (for pediatric-focused opening) This opportunity offers the chance to join a collaborative clinical research team supporting innovative studies while maintaining an excellent work-life balance with daytime weekday hours.