Clinical Research Coordinator - Oxford, MS

IQVIA • Parsippany, NJ

2d • $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.

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees