Job Summary: Join a growing clinical research organization as a Clinical Research Coordinator and play a key role in advancing Phase II-IV clinical trials. We're seeking detail-oriented professionals with 1+ year of clinical research experience who are passionate about patient care, regulatory compliance, and delivering high-quality research. Multiple full-time openings are available, including Adult and Pediatric Clinical Research Coordinator positions for candidates with pediatric research experience. Competitive pay, weekday schedule, and excellent training and growth opportunities offered.

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.