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
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.
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
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
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
High School Diploma and 1 year of relevant clinical research experience
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
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.
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
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
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
Visit https://jobs.iqvia.com and search for Job ID: R1494386, or click Apply Now directly from the posting.
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