Instagram
youtube
Facebook

Site Research Assistant - Winter Park, Fl

1+ years
$25.00 – $39.00 per hour
10 Oct. 16, 2025
Job Description
Job Type: Part Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Position: Site Research Assistant

📍 Location: Winter Park, Florida (Office-based)
🕒 Employment Type: Part-Time
💼 Job ID: R1508699
📅 Scheduled Hours: 24 hours/week


About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.
🔗 Learn more: https://jobs.iqvia.com


Job Overview

The Site Research Assistant plays a key role in assisting with clinical trial activities in compliance with all applicable regulations. This role requires logical thinking, prioritization skills, adaptability, and strong interpersonal and team-building abilities.


Responsibilities

Clinical Trial Support

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

  • Assist with screening, recruiting, and enrollment of research subjects.

  • Collect patient/research participant history.

  • Coordinate follow-up care and laboratory procedures.

  • Support the informed consent process.

  • Ensure the safety of research subjects.

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

  • Adhere to IRB-approved protocols.

  • Schedule subject visits and procedures.

Relationship Management

  • Develop strong working relationships with study team members, investigators, and clinic staff.

  • Build a foundation of trust and respect between clinic and research office.

Compliance

  • Follow company and Sponsor policies, SOPs, and guidelines.

  • Maintain knowledge of protocol-specific procedures, consent forms, and study schedules.


Qualifications

  • Minimum Associate’s Degree or equivalent education/experience.

  • At least 1 year experience in a clinical research setting preferred.

  • Working knowledge of clinical trials and Good Clinical Practices (GCP).

  • Knowledge of protocols, SOPs, consent forms, and study schedules.

  • Skilled in carrying out required clinical procedures.

  • Knowledge of medical terminology.

  • Strong attention to detail and organizational skills.

  • Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.

  • Applicable certifications/licenses as required by company, state, or regulatory bodies.

⚠️ Note: This position is not eligible for sponsorship.


Compensation & Benefits

  • Base pay range: $25.00 – $39.00 per hour (dependent on qualifications, experience, and schedule).

  • May include incentives, bonuses, and other benefits depending on position.


Equal Opportunity

IQVIA is an equal opportunity employer. All qualified applicants receive consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status.
🔗 Equal Opportunity Statement


📩 Apply Now: IQVIA Careers – Site Research Assistant