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Site Research Assistant - Katy, Tx

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: Katy, Texas (On-site)
Job Type: Part-Time (24 hours/week) | Office-Based
Requisition ID: R1497170
Company: IQVIA

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


Position Summary:
IQVIA is seeking a Site Research Assistant to support clinical trial operations on-site in Katy, TX. This role is ideal for individuals with prior clinical research experience who excel in communication, adaptability, and maintaining compliance in a fast-paced environment.


Key Responsibilities:

  • Perform EDC data entry and resolve queries accurately and on time

  • Coordinate with investigators and office staff to build a collaborative, trust-based relationship

  • Assist in screening, recruiting, and enrolling clinical trial participants

  • Schedule and manage participant visits and follow-ups

  • Collect patient histories and manage documentation

  • Support IRB-approved protocol adherence and informed consent processes

  • Ensure participant safety and compliance with regulatory and sponsor guidelines

  • Execute protocol-related procedures, visits, and sample handling


Qualifications:

  • High School Diploma or equivalent, with 1+ year of relevant clinical research experience

  • Familiarity with Good Clinical Practices (GCP) and clinical trial processes

  • Knowledge of medical terminology and protocol-specific documentation

  • Attention to detail and ability to manage multiple tasks under tight deadlines

  • Strong interpersonal, organizational, and communication skills

  • Relevant certifications/licenses as required by regulatory authorities

  • Must be eligible to work in the U.S. (Sponsorship is not available)