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Clinical Research Coordinator

Job

York Clinical Research LLC

Norfolk, VA (In Person)

Full-Time

Posted 3 weeks ago (Updated 2 weeks ago) • Actively hiring

Expires 7/12/2026

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Job Description

Clinical Research Coordinator York Clinical Research LLC Norfolk, VA Job Details Part-time | Full-time 1 hour ago Benefits Paid time off Qualifications Clinical research Clinical development Data management Organizational skills Clinical trials Medical terminology Full Job Description Job Overview We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team in a full-time or part-time capacity. This role is crucial in managing clinical trials and ensuring compliance with regulatory requirements. The ideal candidate will have a strong understanding of medical terminology, clinical development, and Good Clinical Practice (GCP). As a Clinical Research Coordinator, you will play a key role in the planning, execution, and oversight of clinical research studies. Duties Coordinate and oversee all aspects of clinical research studies from initiation to completion. Ensure compliance with GCP, regulatory guidelines, and institutional policies. Manage data collection processes and maintain accurate documentation throughout the study. Conduct documentation reviews to ensure data integrity and accuracy. Analyze study data and prepare reports for stakeholders Perform phlebotomy procedures when required for sample collection. Facilitate communication between study participants, investigators, and monitors. Maintain a thorough understanding of medical terminology relevant to the studies being conducted.
Qualifications :
Experience in clinical research Strong knowledge of medical terminology and clinical development processes. Familiarity with Good Clinical Practice (GCP) guidelines. Proficient in data management techniques and software applications. Excellent organizational skills with attention to detail. Ability to analyze data effectively and prepare comprehensive reports. Strong interpersonal skills for supervising staff and interacting with study participants. Commitment to maintaining confidentiality and ethical standards in research practices. Current GCP certification A pleasant demeanor conducive to site harmony Join us in advancing medical science through innovative research!
Benefits:
Paid time off
Work Location:
In person