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Site Research Assistant - Cooper City, Fl

1+ years
$25.00-$39.00 per hour
10 April 29, 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

 

ChatGPT said:

Job Title: Site Research Assistant
Location: Cooper City, Florida
Job ID: R1478121
Job Type: Part Time


Work Set-Up:

On-site
Scheduled Weekly Hours: 40


Job Summary:

The Site Research Assistant plays a vital role in supporting clinical trial operations in compliance with regulatory standards. The ideal candidate will demonstrate logical thinking, adaptability, strong interpersonal skills, and a collaborative mindset.


Responsibilities:

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

  • Foster effective communication with study team members

  • Build trust-based relationships with investigators and clinic staff

  • Assist with patient screening, recruitment, and enrollment

  • Manage participant scheduling and history collection

  • Coordinate follow-up care and lab procedures

  • Ensure adherence to IRB-approved protocols

  • Support informed consent process and patient safety

  • Execute protocol-specific procedures and follow-up

  • Comply with SOPs, company, and sponsor guidelines

  • Organize subject visit and procedure schedules


Qualifications:

  • High School Diploma with 1 year of relevant clinical research experience (or equivalent education and experience)

  • Preferably 1 year of hands-on experience in a clinical research setting

  • Knowledge of clinical trial practices and Good Clinical Practices (GCP)

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

  • Competency in clinical procedures and medical terminology

  • Attention to detail and strong organizational skills

  • Ability to maintain professional relationships with internal and external stakeholders

  • Certifications/licenses as per regulatory and company requirements

  • Note: This role is not eligible for visa sponsorship


Compensation:

  • Hourly Rate: $25.00 – $39.00 (based on qualifications, experience, and location)

  • Additional Benefits: May include incentive plans, bonuses, health and welfare benefits


About IQVIA:
IQVIA is a global leader in clinical research, data analytics, and healthcare intelligence. We empower the development and delivery of innovative medical solutions that improve patient outcomes worldwide. Learn more at
IQVIA Careers


Equal Opportunity Employer:
IQVIA provides equal employment opportunities without discrimination based on race, religion, sex, national origin, disability, or any other protected status.