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Clinical Research Coordinator - Savannah, Ga

1+ years
$35.00-$42.00 per hou
10 April 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

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Job Title: Clinical Research Coordinator
Location: Savannah, Georgia
Job ID: R1478120
Job Type: Part Time


Work Set-Up:

On-site
Schedule: Tuesdays, Thursdays, and Saturdays (plus possible additional weekday)
Total Weekly Hours: 24


Responsibilities:

  • Perform phlebotomy and complex clinical procedures (e.g., ECG, spirometry, vital signs)

  • Pediatric care experience required

  • Engage in community outreach initiatives

  • Coordinate clinical research studies under principal investigator supervision

  • Maintain and update nursing practices related to clinical research

  • Ensure participant safety and uphold high care standards

  • Support study activities and logistics, including:

    • Reviewing protocols, CRFs, and EDC systems

    • Preparing study materials and equipment

    • Managing specimen labeling and documentation

    • Planning procedures and volunteer instructions

    • Training and supporting study staff

    • Troubleshooting and ensuring quality control of data

  • Recruit and screen volunteers per inclusion criteria

  • Orient participants to the study, process, and expectations

  • Administer and manage custody of study drugs

  • Accurately collect and report clinical data

  • Report adverse events to investigators

  • Collaborate with study monitors and ensure ICH-GCP compliance


Qualifications:

  • High School Diploma with at least 1 year of relevant clinical research experience (or equivalent education and experience)

  • Prior experience in a clinical research setting preferred

  • Certifications/licenses as per regulatory requirements

  • Proficiency in Good Clinical Practices (GCP) and clinical trial protocols

  • Clinical procedure skills and medical terminology knowledge

  • High attention to detail

  • Strong interpersonal and professional relationship skills

  • Note: This role is not eligible for visa sponsorship


Compensation:

  • Hourly Rate: $35.00 – $42.00 (based on qualifications, experience, and location)

  • Additional Benefits: May include incentives, bonuses, and a variety of health/welfare offerings


About IQVIA:
IQVIA is a global leader in providing clinical research services and healthcare intelligence, helping to advance innovative medical treatments that improve health outcomes worldwide. Learn more at
IQVIA Careers


Equal Opportunity Employer:
IQVIA ensures equal employment opportunity for all, regardless of race, religion, gender, or any other protected status.