Clinical Research Coordinator, On-Site, Kenner, Louisiana

Accelerate clinical research as a Clinical Research Coordinator (CRC) on‑site in Kenner, Louisiana. Join IQVIA, a global leader in clinical research services, and support groundbreaking studies that drive improved patient outcomes.

This role involves coordinating clinical research studies per protocol, ICH‑GCP, sponsor and company SOPs, and local regulations. You will provide patient recruitment, data collection, study monitoring support, and maintain regulatory compliance.

• Coordinate clinical research studies conducted by a supervising principal investigator.
• Assist as backup CRC on other studies.
• Develop and implement patient recruitment strategies; actively recruit to ensure enrollment targets are achieved.
• Obtain informed consent of research subjects.
• Develop strong working relationships and maintain effective communication with study team members.
• Complete all protocol‑related training.
• Perform patient/research participant scheduling.
• Collect patient/research participant history.
• Collect and maintain source documentation.
• Manage inventory and administer test articles/investigational product to participants.
• Perform data entry and query resolution.
• Support the collection and review of required essential study documents and reports.
• Order supportive study supplies (e.g., contracts, IXRS, lab kits, non‑clinical supply materials, imaging, and laboratory handling manuals, etc.).
• Adhere to an IRB approved protocol.
• Support the safety of research subjects and report adverse events.
• Coordinate protocol‑related research procedures, study visits, and follow‑up.
• Facilitate pre‑study, site qualification, study initiation, monitoring visits, and study close‑out activities.
• Collect, process, and ship laboratory specimens.
• May be asked to perform special project responsibilities and travel to other clinic locations within the area when needs arise.
• Comply with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines.
• Perform other duties as assigned.

• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
• Clinical Research Coordinator experience within a similar setting preferred.
• Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
• Knowledge and experience of site operations and the drug development process.
• Effective communication skills.
• Computer proficiency in use of Microsoft Word and Excel.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Learn more at

IQVIA is proud to be an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

The potential base pay range for this role is $0.00 - $0.00. The actual base pay offered may vary based on qualifications, location, and schedule.

Seniority Level: Entry level.

Employment Type:

Full‑time.

Job Function:
Research, Analyst & Information Technology.

Industries:
Hospitals and Health Care.