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
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