Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Site Research Assistant - Kenosha, Wi

Iqvia
IQVIA
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