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
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.
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
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
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
High School Diploma or equivalent
At least 1 year of relevant clinical research experience
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
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.
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.
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
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
Search Job ID: R1484968 at https://jobs.iqvia.com or use the Apply Now link directly from the job listing.
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