Clinical Research Coordinator

Role Summary The Clinical Research Coordinator develops and maintains effective relationships with study investigators, healthcare professionals, and team members to support clinical research activities. They ensure compliance with Good Clinical Practices (CFR 21), FDA, IRB, and ethical guidelines in conducting research studies. Key Responsibilities Collaborate with investigators and healthcare staff to facilitate research processes.Ensure adherence to regulatory standards and ethical principles.Support data collection, study documentation, and participant management.Maintain professional behavior aligned with organizational mission and values. Qualifications & Skills Bachelor’s Degree in a related field or equivalent experience/education.At least 2 years of related clinical research experience or equivalent qualifications.Preferred: Certification in Clinical Research within 2 years, BLS certification within 6 months, and 2 years of clinical trial experience. Additional Information The role offers a comprehensive benefits package, opportunities for professional growth, and a supportive, inclusive work environment. Candidates' compensation will be based on experience and other relevant factors.