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Clinical Research Coordinator - Smyrna, Ga

1 year years
$35.00 – $42.00
10 Aug. 29, 2025
Job Description
Job Type: Part Time Education: High School Diploma and 1 year of relevant clinical research experience 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: Smyrna, Georgia
Job Type: Part-Time
Work Set-Up: On-Site (Office-Based)
Weekly Hours: 20 hours/week
Job ID: R1494386
Company: IQVIA
Availability: Also available in additional locations


Position Summary:

This on-site Clinical Research Coordinator role is ideal for a detail-oriented, patient-focused professional with experience in phlebotomy and pediatric care. You will be instrumental in coordinating and executing clinical trial activities while maintaining strict adherence to Good Clinical Practices (GCP), safety regulations, and study protocols.


Key Responsibilities:

Clinical Operations:

  • Perform a variety of complex clinical procedures including:

    • Phlebotomy

    • Pediatric sample collection

    • ECGs, spirometry, and vital signs

  • Safeguard the well-being of study subjects by:

    • Maintaining a safe environment per Health and Safety policies

    • Acting as a volunteer advocate

    • Addressing concerns proactively

  • Administer and monitor investigational products per protocol

  • Conduct community outreach as part of subject recruitment

Study Coordination:

  • Coordinate clinical studies under a supervising principal investigator

  • Maintain up-to-date knowledge of nursing and clinical research best practices

  • Participate in study set-up and planning:

    • Review study protocols, CRFs, and EDC systems

    • Label and prepare specimen containers

    • Set up equipment and study documentation

    • Plan logistical tasks for procedures

  • Recruit and screen volunteers based on inclusion/exclusion criteria

  • Orient participants to the study, including objectives and visit timelines

  • Schedule and coordinate study visits and procedures

Data Management & Compliance:

  • Enter, review, and resolve queries in clinical databases

  • Ensure adherence to ICH GCP, protocols, SOPs, and regulatory guidelines

  • Accurately record and report data in CRFs

  • Monitor and report adverse events (AEs) and serious adverse events (SAEs)

  • Assist with quality control, data accuracy, and content completeness

  • Support monitor visits and respond to questions from study monitors


Qualifications:

Minimum Requirements:

  • High School Diploma and 1 year of relevant clinical research experience

Preferred:

  • At least 1 year of experience in a clinical research setting

  • Pediatric care and phlebotomy experience strongly preferred

  • Applicable certifications/licenses as required by local, state, or national regulations

Skills & Competencies:

  • Knowledge of clinical trials, GCP principles, and medical terminology

  • Proficient in executing study-specific procedures and protocols

  • Strong attention to detail and ability to multitask

  • Excellent interpersonal and communication skills

  • Able to collaborate with investigators, staff, patients, and sponsors

🔒 Note: This position is not eligible for employer-sponsored work visa support.


Compensation:

  • Hourly Pay Range: $35.00 – $42.00
    (Actual pay may vary depending on qualifications, experience, and location.)

  • May be eligible for bonuses, incentives, and a benefits package


About IQVIA:

IQVIA is a global leader in advanced analytics, clinical research, and technology solutions, helping healthcare and life sciences clients innovate and improve patient outcomes.
🔗 Learn more at: https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA is committed to providing equal employment opportunities to all applicants regardless of race, religion, gender, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status.
🔗 Read our EEO policy: https://jobs.iqvia.com/eoe


How to Apply:

Visit https://jobs.iqvia.com and search for Job ID: R1494386, or click Apply Now directly from the posting.