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Clinical Research Coordinator - New York, Ny

1 year years
$35.00 – $42.00
10 Aug. 29, 2025
Job Description
Job Type: Part Time Education: High School Diploma (or equivalent) 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: 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


Position Overview:

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.


Key Responsibilities:

Clinical Duties:

  • 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

Study Coordination:

  • 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

Study Support:

  • 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

Compliance & Quality:

  • 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


Qualifications:

  • 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.


Compensation:

  • 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.


About IQVIA:

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


Equal Opportunity Employer Statement:

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


How to Apply:

Use Job ID: R1499501 or apply directly through the IQVIA careers website.