Location: New York, NY
Job Type: Part-Time
Work Arrangement: On-Site (Office-Based)
Schedule: 24 hours per week
Job ID: R1499501
Company: IQVIA
Also Available In: Additional locations
The Clinical Research Coordinator (CRC) supports the planning and execution of clinical research studies in accordance with ICH-GCP guidelines, protocol requirements, and regulatory policies. This role involves hands-on clinical duties, community outreach, and pediatric care.
Perform clinical procedures including:
Phlebotomy (required)
Pediatric care (required)
ECGs, spirometry, vital signs, and sample collection
Ensure patient safety and advocacy throughout the study
Maintain a clean, safe, and compliant work environment
Administer and manage investigational products per protocol
Coordinate and execute study procedures under the supervision of a principal investigator
Participate in all phases of clinical trials from initiation to close-out
Recruit and screen volunteers per study inclusion/exclusion criteria
Obtain informed consent from research participants
Orient participants to study protocols and visit expectations
Conduct community outreach for participant recruitment
Prepare study supplies, documents, and training materials
Review study protocols and case report forms (CRFs)
Set up equipment and manage study-specific logistics
Label and prepare specimen collection containers
Manage data entry, data quality review, and query resolution
Attend team huddles and project meetings
Troubleshoot and resolve study-related issues
Follow ICH-GCP guidelines and all applicable regulations
Collaborate with monitors during site visits and audits
Document and report adverse events (AEs/SAEs)
Maintain detailed and accurate CRFs and source documentation
Education: High School Diploma (or equivalent)
Experience:
Minimum 1 year of clinical research experience preferred
Pediatric and phlebotomy experience required
Knowledge & Skills:
Working knowledge of clinical trials and GCP/ICH guidelines
Familiarity with medical terminology and standard clinical procedures
Excellent organizational skills with attention to detail
Ability to work collaboratively with staff, patients, and physicians
Certifications/Licenses:
Must hold relevant certifications or licenses as required by local/state regulations
Sponsorship: This position is not eligible for work visa sponsorship.
Hourly Pay Range: $35.00 – $42.00
(Based on experience, education, location, and schedule)
May include bonuses, incentive plans, and other compensation/benefits as eligible.
IQVIA is a global leader in clinical research, real-world evidence, and healthcare analytics, accelerating innovation to improve patient outcomes and public health.
🔗 Learn more: https://jobs.iqvia.com
IQVIA provides equal employment opportunities without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
🔗 Learn more: https://jobs.iqvia.com/eoe
Use Job ID: R1499501 or apply directly through the IQVIA careers website.
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Brazil | Sao paulo |Attica :
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