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Site Research Assistant - Kenosha, Wi

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: Kenosha, Wisconsin (On-site)
Job Type: Part-Time | 24 hours/week | Office-Based
Requisition ID: R1495515
Company: IQVIA

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


Position Overview:
IQVIA is seeking a dedicated Site Research Assistant to support the execution of clinical trials at our Kenosha, WI site. This role is ideal for professionals with strong interpersonal skills, attention to detail, and a passion for advancing clinical research. You will work closely with investigators, clinical teams, and study participants, contributing to each stage of the clinical trial process.


Key Responsibilities:

  • Enter Electronic Data Capture (EDC) data and resolve queries

  • Collaborate with investigators and clinical staff to build strong working relationships

  • Assist in screening, recruiting, and enrolling research participants

  • Schedule patient visits and manage participant follow-up

  • Collect participant history and coordinate lab procedures

  • Ensure compliance with IRB-approved protocols and GCP guidelines

  • Support the informed consent process

  • Assist with protocol-related procedures and data collection

  • Maintain adherence to sponsor and company SOPs and study guidelines


Qualifications:

  • High School Diploma with at least 1 year of clinical research experience (required)

  • Strong working knowledge of clinical trial processes and GCP principles

  • Familiarity with study protocols, informed consent forms, and visit schedules

  • Basic clinical procedure experience (preferred)

  • Understanding of medical terminology

  • High attention to detail and strong organizational skills

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

  • Certifications and licenses as applicable per company/state requirements

  • Sponsorship is not available for this position