Clinical Research Coordinator
IQVIA • Parsippany, MS6d • $35 - $42 • Onsite
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Clinical Research Coordinator - Oxford, MS
IQVIA•Parsippany, MS
•$35 - $42•Onsite
About The Position
IQVIA is seeking a Clinical Research Coordinator (CRC) to support the execution of clinical research studies at our Oxford, MS site. Under the supervision of a Principal Investigator, this role plays a critical part in patient-facing study activities, regulatory compliance, and high-quality data collection. This is an excellent opportunity for an experienced CRC who enjoys hands-on clinical work, patient interaction, and contributing to well-conducted clinical trials in a collaborative onsite environment.
Requirements
- Prior experience as a Clinical Research Coordinator or in a similar clinical research role.
- Minimum 1+ year of relevant clinical research experience , including direct involvement in patient visits.
- Demonstrated experience performing phlebotomy and other clinical procedures.
- Working knowledge of clinical trial conduct, GCP guidelines, and medical terminology.
- Proficiency with EDC systems, accurate data entry, and query management.
- Strong attention to detail, organizational skills, and the ability to build effective working relationships.
Nice To Haves
- Bachelor’s degree in a science, healthcare, or related field, or an equivalent combination of education and experience.
Responsibilities
- Conduct in-person study visits , ensuring protocol adherence and patient safety throughout participation.
- Perform clinical procedures including phlebotomy, ECGs, vital signs, and specimen collection .
- Coordinate daily study activities, including preparation of study materials, equipment setup, and visit logistics.
- Recruit, screen, consent, and orient study participants while maintaining a patient-centered approach.
- Accurately collect and enter clinical data into electronic data capture (EDC) systems and resolve data queries.
- Maintain compliance with study protocols, Good Clinical Practice (GCP) , and regulatory requirements.
- Collaborate closely with investigators, clinical monitors, and site staff to support successful study execution.
- Serve as a patient advocate and promote a safe, compliant clinical research environment in line with Health & Safety policies.
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
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