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Clinical Research Coordinator

1 years
$35.00 – $42.00
10 Sept. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.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

Job Title:

Clinical Research Coordinator


Location:

Hollywood, Florida
Office-based / On-site


Work Schedule:

  • Part-time

  • 24 hours per week

  • On-site work setup


Job ID:

R1503632


Compensation:

  • Hourly pay range: $35.00 – $42.00

  • Actual pay dependent on:

    • Qualifications (knowledge, skills, education, experience)

    • Location

    • Schedule (full-time/part-time)

  • May include incentives, bonuses, and additional benefits


Key Responsibilities:

Clinical Procedures & Patient Care

  • Perform phlebotomy (including pediatric patients)

  • Conduct complex clinical procedures such as ECGs, spirometry, vital signs, and sample collection

  • Ensure safety and well-being of research subjects following Health & Safety policies

  • Act as volunteer advocate and address concerns proactively

  • Assist staff in delivering care and clinical coordination

  • Report deviations from standard practice to senior staff

Study Coordination & Support

  • Coordinate clinical research studies under supervision of principal investigator

  • Review study protocols, case report forms (CRFs), and related documents

  • Participate in project team meetings and daily huddles

  • Prepare clinical setups including labeling specimens, setting up equipment and documents

  • Plan and execute study procedures according to protocol

  • Generate volunteer instructions and identify necessary supplies

  • Prepare and deliver study-specific training materials

  • Troubleshoot issues during study conduct

  • Recruit, screen, and orient volunteers to the study and site

  • Administer and custody study drugs per SOPs

Data Management & Compliance

  • Collect, record, and report clinical data accurately in CRFs

  • Collaborate with study investigators to report adverse and serious adverse events

  • Assist with data quality control and query resolution

  • Cooperate with study monitors during monitoring visits

  • Follow ICH GCP guidelines and site SOPs for all study activities


Qualifications:

Minimum Education & Experience

  • High School Diploma (or equivalent)

  • Minimum 1 year relevant clinical research experience

Preferred Experience

  • At least 1 year clinical research setting experience

  • Pediatric and community outreach experience

Required Skills & Knowledge

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

  • Understanding of protocols, consent forms, study schedules

  • Skilled in clinical procedures

  • Familiarity with medical terminology

  • Strong attention to detail

  • Ability to build and maintain effective relationships with coworkers, patients, and stakeholders

Certifications & Licenses

  • Must hold applicable certifications/licenses as required by company, regulatory bodies, state, or country


Additional Information:

  • This position is not eligible for sponsorship

  • Tags: #LI-CES, #LI-DNP, #LI-HCP, #ONSITE


About IQVIA:

IQVIA is a global leader in clinical research services, healthcare intelligence, and life sciences consulting, dedicated to accelerating innovation and improving patient outcomes worldwide.

Learn more: https://jobs.iqvia.com
Equal Opportunity Employer: https://jobs.iqvia.com/eoe


Application:

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