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Site Research Assistant - Hallandale Beach, Fl

1 year years
$25.00 – $39.00/hour
10 Aug. 29, 2025
Job Description
Job Type: Part Time Education: Minimum of an Associate’s degree 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: Hallandale Beach, FL (Office Based)
Nearby Location: Aventura, Florida
Job Type: Part-Time
Work Arrangement: On-Site
Weekly Hours: 24 hours/week
Job ID: R1499274
Company: IQVIA
Also Available In: Additional locations


Position Summary:

The Site Research Assistant plays a critical role in supporting clinical trial activities in compliance with regulatory guidelines and protocols. This role emphasizes collaboration, adaptability, and organizational efficiency within a patient-centered research environment.


Key Responsibilities:

Clinical Trial Support:

  • Perform Electronic Data Capture (EDC) entry and query resolution

  • Coordinate patient/research participant scheduling

  • Assist with screening, recruiting, and enrolling study participants

  • Collect patient medical history and relevant documentation

  • Coordinate follow-up care and lab procedures

  • Maintain compliance with IRB-approved protocols

  • Assist in the informed consent process

  • Support and ensure participant safety

  • Coordinate protocol-related procedures, study visits, and follow-up care

Relationship Management:

  • Develop and maintain effective communication with study team members

  • Build strong working relationships with investigators and clinic staff

Compliance and Administration:

  • Adhere to company and sponsor SOPs, guidelines, and policies

  • Schedule participant visits and required study procedures


Qualifications:

  • Education: Minimum of an Associate’s degree required

  • Experience:

    • Minimum 1 year of clinical research experience preferred

  • Skills & Knowledge:

    • Understanding of clinical trials and GCP (Good Clinical Practice) principles

    • In-depth knowledge of study protocols, operating procedures, consent forms, and visit schedules

    • Competence in performing required clinical procedures

    • Familiarity with medical terminology

    • Exceptional attention to detail

    • Ability to build effective relationships with colleagues, patients, physicians, and managers

  • Certifications/Licenses: Must meet any certification or licensure requirements as required by state, country, company, or other regulatory bodies

  • Sponsorship: This position is not eligible for work visa sponsorship


Compensation:

  • Hourly Pay Range: $25.00 – $39.00/hour
    (Pay is based on education, experience, location, and work schedule)

  • May include:

    • Performance-based bonuses

    • Incentive plans

    • Health and welfare benefits, depending on role and eligibility


About IQVIA:

IQVIA is a global leader in clinical research and healthcare analytics, creating data-driven solutions to accelerate innovation in medical development and improve global health outcomes.
🔗 Learn more: https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA is an Equal Opportunity Employer. All applicants will be considered for employment without discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected status.
🔗 EEO Statement: https://jobs.iqvia.com/eoe


How to Apply:

Apply using Job ID: R1499274 via the IQVIA Careers Site