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Clinical Research Coordinator, On-Site, Metairie, Louisiana

0-2 years
$36,600.00 - $91,300.00
10 Aug. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Coordinator – On-Site
Location: Metairie, Louisiana (Relocating to Kenner, Louisiana after September 2025)
Job Type: Full-Time | Office-Based
Requisition ID: R1495981
Company: IQVIA

Salary:
$36,600 – $91,300 annually
(Actual compensation will vary depending on skills, qualifications, location, and experience. Additional benefits and bonuses may be included.)


Position Overview:
IQVIA is seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to join our dynamic, patient-focused research team in Metairie, Louisiana. This on-site role involves supporting and managing clinical research activities to ensure adherence to study protocols, regulatory guidelines, and company standards. The site will relocate to Kenner, Louisiana after September 2025, and the position will remain fully on-site.


Key Responsibilities:

  • Coordinate studies conducted by a Principal Investigator (PI)

  • Act as a backup CRC on other trials when needed

  • Develop and execute recruitment strategies to meet enrollment targets

  • Obtain informed consent and collect participant history

  • Schedule and conduct protocol-related study visits

  • Perform data entry, resolve queries, and maintain accurate source documentation

  • Administer investigational product and manage study inventory

  • Process and ship lab specimens

  • Ensure compliance with IRB protocols and safety standards

  • Attend study initiation, monitoring, and closeout visits

  • Collaborate with sponsors, monitors, and cross-functional team members

  • May be required to travel locally to support additional sites


Required Qualifications:

  • Knowledge of ICH-GCP and applicable regulatory requirements

  • Clinical Research Coordinator experience preferred

  • Clinical skills including vital signs, phlebotomy, and EKG preferred

  • Proficiency in Microsoft Word and Excel

  • Strong communication, organization, and problem-solving skills

  • Ability to multitask in a fast-paced, research-focused environment


Preferred Attributes:

  • Prior experience in a clinical research site setting

  • Familiarity with drug development processes

  • Willingness to grow within the organization and take on new challenges