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Clinical Research Coordinator

1 years
$35.00 โ€“ $42.00
10 Sept. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.Pharma/ Life Sciences 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

๐Ÿท๏ธ Job Title:

Clinical Research Coordinator

๐Ÿ“ Location:

Elgin, Illinois
Job ID: R1503866
Job Type: Part-Time (24 hours/week)
Work Setup: Office-based (On-site)
Job available in additional locations

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๐Ÿงญ Overview

Join IQVIA’s clinical research team in Elgin, IL as a Clinical Research Coordinator. In this part-time, on-site role, you'll support the coordination and execution of clinical studies with a strong focus on patient care, safety, and protocol compliance. Phlebotomy, pediatric experience, and community outreach are key aspects of this role.


๐Ÿ”‘ Key Responsibilities

๐Ÿฉบ Clinical Procedures & Patient Care

  • Perform phlebotomy and pediatric procedures

  • Conduct ECGs, spirometry, vital signs, and other complex clinical procedures

  • Support patient recruitment, screening, and study enrollment

  • Coordinate protocol-related study visits and follow-up care

  • Obtain informed consent and ensure volunteer safety

  • Act as a patient/volunteer advocate and uphold a safe environment

๐Ÿ“ Study Conduct & Coordination

  • Review study protocols, CRFs, and related documents

  • Prepare clinical setups, label specimen containers, and manage supplies

  • Execute logistical planning and procedure scheduling

  • Deliver study-specific training materials and instructions

  • Assist in community outreach and volunteer engagement

  • Participate in study team meetings and daily huddles

๐Ÿ“Š Data Management & Quality

  • Collect, record, and report clinical data in CRFs and EDC systems

  • Perform data quality checks and resolve queries

  • Follow ICH-GCP guidelines and site SOPs

  • Report adverse events (AEs/SAEs) per protocol and regulatory requirements

  • Support study monitoring visits and collaborate with study monitors


๐ŸŽ“ Qualifications

Required:

  • High School Diploma or equivalent

  • At least 1 year of relevant clinical research experience

  • Phlebotomy experience required

  • Pediatric clinical experience preferred

  • Experience with community outreach initiatives

Skills & Knowledge:

  • Working knowledge of clinical trials and GCP principles

  • Proficient in medical terminology and clinical procedures

  • Detail-oriented with excellent organizational skills

  • Strong interpersonal and communication abilities

  • Able to build effective working relationships with patients, teams, and investigators

Certifications:

  • Applicable certifications and licenses as required by local/state/country regulations

Note: This position is not eligible for visa sponsorship.


๐Ÿ’ต Compensation & Benefits

  • Hourly Pay Range: $35.00 – $42.00

  • Final compensation will vary based on experience, education, and skills

  • Eligible for potential bonuses, incentive plans, and a range of health/welfare benefits


๐ŸŒ About IQVIA

IQVIA is a global leader in clinical research, healthcare analytics, and technology-driven solutions for life sciences. We power better decision-making through data-driven insights and aim to improve health outcomes worldwide.

๐Ÿ”— Learn more at: https://jobs.iqvia.com


โš–๏ธ Equal Opportunity Employer

IQVIA provides equal employment opportunities to all employees and applicants. We do not discriminate based on race, color, religion, gender, sexual orientation, gender identity, national origin, disability, protected veteran status, or any legally protected status.

๐Ÿ”— EEO Policy


๐Ÿ“ฉ Ready to Apply?

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