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Site Research Assistant - Hammond, La

1+ years
$25.00-$39.00 per hour
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

Site Research Assistant – Part-Time
Location: Covington, Louisiana (On-site for Hammond, LA Site)
Job Type: Part-Time (24 hours/week) | Office-Based
Requisition ID: R1485908
Company: IQVIA

Salary:
$25.00 – $39.00 per hour
(Compensation may vary based on qualifications, experience, and location. Additional benefits or incentives may apply.)


Position Overview:
IQVIA is hiring a Site Research Assistant to support clinical trial operations in Hammond, Louisiana, while being based on-site in Covington, LA. This is a great opportunity for individuals with experience or interest in clinical research to join a collaborative team and contribute to cutting-edge healthcare studies. This role is ideal for candidates who are detail-oriented, adaptable, and possess strong communication skills.


Key Responsibilities:

  • Perform EDC data entry and query resolution

  • Coordinate with investigators and site staff to ensure smooth study operations

  • Assist in screening, recruitment, and enrollment of trial participants

  • Schedule patient visits and collect participant history

  • Support follow-up care and lab coordination

  • Help with the informed consent process and ensure protocol adherence

  • Maintain compliance with IRB protocols, SOPs, GCP, and study-specific guidelines

  • Ensure subject safety and quality documentation of study procedures


Qualifications:

  • High School Diploma with at least 1 year of relevant work experience in clinical research

  • Prior experience in a clinical trial setting preferred

  • Strong understanding of GCP principles and clinical protocols

  • Proficient in medical terminology and clinical procedures

  • Attention to detail and effective communication skills

  • Ability to work collaboratively with patients, physicians, and team members

  • Must meet applicable certification and licensing requirements