Clinical Research Coordinator

Job Summary
We are seeking an experienced Clinical Research Coordinator to join our growing research team. The Clinical Research Coordinator plays a pivotal role in the management and execution of clinical trials. This position involves overseeing the day-to-day operations of research studies, managing all aspects of assigned clinical trials in accordance with Good Clinical Practice (GCP), FDA regulations, IRB policies and internal standard operating procedures (SOP's). This role requires a detail-orientated, organized professional that thrives in a fast- paced environment and has strong interpersonal and problem -solving skills.

Duties

• Coordinate and manage all aspects of assigned clinical trials from initiation through close out.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Conduct patient recruitment, prescreening, screening, and informed consent processes.
• Serve as the primary liaison between sponsors, CRO's, monitors and internal staff.
• Monitor patient progress throughout the study, documenting any adverse events or changes in condition.
• Collect, record and maintain accurate source documentation and case report forms.
• Prepare for and participate in monitoring visits, audits and inspections
• Maintain comprehensive records of study activities, including medical terminology relevant to the research.
• Collaborate with physicians, nurses, and other healthcare professionals to facilitate effective communication regarding study protocols.

Qualifications

• Bachelor’s degree in a relevant field; nursing experience is a plus.
• Strong understanding of clinical development processes and regulatory requirements.
• Proficient in medical terminology and data collection methodologies.
• Ability to perform blood sampling and phlebotomize patients safely and effectively is a plus.
• Ability to manage multiple studies with minimal supervision from leadership.
• Excellent organizational skills with the ability to supervise staff effectively.
• Strong communication skills to interact with patients, healthcare professionals, and research teams.
• Prior experience in a clinical research setting is highly desirable.
• Certified Clinical Research Coordinator (CCRC) preferred.

This role is essential for advancing medical knowledge through rigorous research practices while ensuring the safety and well-being of participants involved in clinical trials.

Job Type: Full-time

Pay: $20.00 - $24.00 per hour

Expected hours: 40 per week

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off

Work Location: In person