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OrthoCarolina Research Institute seeks a Clinical Research Coordinator to conduct clinical trial activities under supervision, ensuring accuracy and timeliness. Responsibilities include adherence to FDA regulations, ICH Guidelines, GCP, and OCRI SOPs, with data capture and regulatory duties supported by a senior staff member.
A Bachelor’s degree is required, and CCRC certification is preferred. We offer a collaborative, research-driven environment with opportunities for career growth,
The OrthoCarolina Research Institute (OCRI) is an independent, non-profit 501(c)(3) uniquely positioned as both an academic research center and clinical research site servicing industry research. Research conducted at the OrthoCarolina Research Institute allows the physicians of OrthoCarolina, PA to offer the best available options, treatments, and cost savings identified through evidence-based research. Our research findings are repeatedly published worldwide for the betterment of orthopedics. If you have the desire to work for an organization that is dedicated to raising the bar through research that facilitates the advancement of orthopedics and educating the medical community, while improving the quality of life for patients – then the OrthoCarolina Research Institute (OCRI) is looking for you to join our team as a Clinical Research Coordinator. The role of Clinical Research Coordinator is responsible for completing clinical trial assignments in an accurate and timely manner under the close supervision of a senior staff member. The Clinical Research Coordinator will carry out all research activities according to Food and Drug Administration (FDA) regulations, ICH Guidelines, Good Clinical Practices (GCP) and OCRI standard operating procedures.
A Bachelor of Science or Bachelor of Arts degree. Professional license or certification requirements: Clinical Research Coordinator certification (CCRC) preferred.
Employee Type Regular Qualifications Skills Education B.S. Certifications Language English Work Experience
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