Clinical Research Coordinator
About The Position
Make a Difference Through Clinical Research Are you passionate about advancing medicine and improving patient care? We are seeking a detail-oriented, organized, and compassionate Clinical Research Coordinator (CRC) to join our growing research team. This is an exciting opportunity to work alongside physicians, sponsors, and participants to help bring innovative treatments to patients. Position Summary The Clinical Research Coordinator is responsible for coordinating all aspects of clinical research studies while ensuring compliance with federal regulations, Good Clinical Practice (GCP), and study protocols. The ideal candidate is an excellent communicator who thrives in a fast-paced healthcare environment and is committed to delivering exceptional patient care.
Requirements
- Bachelor's degree in a health science or clinical healthcare experience.
- Strong organizational and time management skills.
- Excellent interpersonal and communication abilities.
- Ability to manage multiple studies while maintaining attention to detail.
- Proficiency with electronic medical records and Microsoft Office applications.
Nice To Haves
- Knowledge of GCP, FDA Regulations, and human subject protection beneficial, but not necessary.
- Compassionate and patient-focused
- Highly organized and detail-oriented
- A strong communicator and team player
- Adaptable and able to prioritize competing responsibilities
- Self-motivated with excellent problem-solving skills
- Committed to quality and regulatory compliance
Responsibilities
- Coordinate and manage clinical research studies from start-up through close-out.
- Recruit, screen, and enroll study participants.
- Schedule and conduct study visits according to protocol requirements.
- Obtain informed consent and educate participants on study procedures.
- Collect, document, and maintain accurate study data and source documentation.
- Ensure compliance with FDA regulations, ICH-GCP guidelines, and institutional policies.
- Communicate effectively with sponsors, monitors, investigators, and research participants.
- Prepare for monitoring visits, audits, and regulatory inspections.
- Manage study supplies and maintain regulatory binders.
Benefits
- Competitive salary and comprehensive benefits package.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
