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Site Research Assistant - Merrillville, In

1 year years
Not Disclosed
10 Aug. 29, 2025
Job Description
Job Type: Part Time Education: Minimum: High School Diploma + 1 year of relevant clinical research experience 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

Job Title: Site Research Assistant

Location: Merrillville, Indiana
Job Type: Part-Time
Scheduled Weekly Hours: 40 Hours
Work Set-Up: On-Site (Office-Based)
Job ID: R1501506
Availability: Also available in additional locations
Company: IQVIA


Position Overview:

The Site Research Assistant plays a critical role in supporting the conduct of clinical trials in compliance with regulatory and institutional guidelines. This role involves patient interaction, data entry, protocol adherence, and administrative coordination. The ideal candidate is organized, detail-oriented, and able to adapt in a fast-paced environment.


Key Responsibilities:

Clinical Support & Coordination

  • Assist in the screening, recruiting, and enrollment of clinical research participants.

  • Schedule research participants for study-related procedures and follow-up care.

  • Collect and document medical and research histories.

  • Coordinate and carry out study visits and protocol-related procedures.

Data Management

  • Perform Electronic Data Capture (EDC) entry and resolve data queries accurately.

  • Maintain accurate and organized source documentation.

Protocol & Compliance

  • Adhere to IRB-approved study protocols and Good Clinical Practice (GCP) standards.

  • Assist in the informed consent process.

  • Ensure participant safety throughout the study.

  • Comply with sponsor and company SOPs, policies, and applicable regulations.

Collaboration & Communication

  • Foster effective communication with investigators, office staff, and study teams.

  • Build strong relationships to support seamless clinical operations and team cohesion.


Qualifications:

  • Education & Experience:

    • Minimum: High School Diploma + 1 year of relevant clinical research experience.

    • Preferred: At least 1 year of hands-on experience in a clinical research setting.

  • Skills & Knowledge:

    • Working knowledge of clinical trials and GCP principles.

    • Familiarity with study protocols, consent forms, and clinical procedures.

    • Strong attention to detail and organizational skills.

    • Ability to perform required clinical procedures.

    • Effective communication and interpersonal skills.

    • Understanding of medical terminology.

  • Certifications & Licenses:

    • Must meet applicable certification or licensing requirements per company, state, and federal regulations.

Note: This position is not eligible for sponsorship.


Compensation & Benefits:

  • Hourly Pay Range: $25.00 – $39.00
    (Final compensation based on experience, education, location, and other job-related factors.)

  • May include bonuses, incentive plans, and a full range of health and welfare benefits.


About IQVIA:

IQVIA is a leading global provider of clinical research, healthcare data analytics, and life sciences solutions. By integrating data, technology, and human expertise, IQVIA supports the development and delivery of innovative medical treatments and health strategies.
Learn more: https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA is committed to creating a diverse and inclusive workplace. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or other legally protected status.
EEO Policy: https://jobs.iqvia.com/eoe


How to Apply:

Visit https://jobs.iqvia.com and search for Job ID: R1501506, or click Apply Now to begin the application process.