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Clinical Research Coordinator - Charleston, Sc

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: Charleston, South Carolina
Job Type: Part-Time
Work Arrangement: On-Site (Office-Based)
Weekly Schedule: 24 hours/week
Job ID: R1484968
Company: IQVIA
Also Available In: Additional locations


Position Summary:

This part-time Clinical Research Coordinator (CRC) position offers an opportunity to contribute to high-impact clinical trials. The ideal candidate will be proficient in clinical procedures including phlebotomy and will have pediatric experience. Community outreach is also an essential part of this role. You’ll be working closely with a principal investigator to ensure accurate, ethical, and efficient conduct of clinical studies.


Key Responsibilities:

Clinical Duties:

  • Perform clinical procedures including:

    • Phlebotomy (required)

    • Pediatric care (required)

    • ECG, spirometry, and vital signs

  • Administer and manage study drugs per SOP

  • Maintain a safe and compliant clinical environment

  • Act as a volunteer advocate, addressing concerns proactively

  • Report any deviation from standard practice

Study Coordination:

  • Coordinate studies under the supervision of a principal investigator

  • Participate in and support:

    • Study set-up and protocol review

    • Labeling and preparation of specimen collection materials

    • Equipment setup and preparation of documents

    • Study-specific training materials

    • Team huddles and daily planning

  • Plan and coordinate logistics for protocol procedures

  • Generate participant instructions and obtain required supplies

  • Attend and support study meetings and site visits:

    • Pre-study, initiation, monitoring, and close-out visits

Participant Engagement & Data Collection:

  • Recruit and screen participants using inclusion/exclusion criteria

  • Obtain informed consent and orient participants to the study process

  • Schedule and conduct study visits and procedures

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

  • Report adverse events (AEs) and serious adverse events (SAEs)

  • Ensure data integrity and resolve queries promptly

  • Collaborate with monitors during site visits


Qualifications:

Minimum Requirements:

  • High School Diploma or equivalent

  • At least 1 year of relevant clinical research experience

Preferred:

  • Pediatric care and phlebotomy experience strongly preferred

  • Familiarity with:

    • Good Clinical Practice (GCP)

    • ICH guidelines

    • Clinical protocols and CRFs

    • Medical terminology

    • Electronic Data Capture (EDC) systems

Skills & Attributes:

  • Excellent attention to detail

  • Strong interpersonal and communication skills

  • Ability to build effective relationships with coworkers, physicians, and patients

  • Ability to perform and document clinical procedures accurately

⚠️ Note: This position is not eligible for sponsorship.


Compensation:

  • Hourly Pay Range: $35.00 – $42.00
    (Pay will vary based on experience, qualifications, and location.)

  • May include bonuses, incentive plans, and health/welfare benefits depending on position and eligibility.


About IQVIA:

IQVIA is a global leader in clinical research services, real-world evidence, and data analytics. We connect healthcare insights and technology to drive better outcomes for patients around the world.
🔗 Visit: https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA welcomes applicants of all backgrounds. We prohibit discrimination based on race, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status, or any other legally protected category.
🔗 Learn more: https://jobs.iqvia.com/eoe


How to Apply:

Search Job ID: R1484968 at https://jobs.iqvia.com or use the Apply Now link directly from the job listing.