Job Title: Clinical Research Coordinator
Location: Kansas City, Missouri (Office-based)
Job ID: R1510792
Employment Type: Part-Time
Work Setup: On-site (40 hours per week)
Additional Locations: Kansas
Overview
IQVIA is seeking a Clinical Research Coordinator to support the execution of clinical research studies under the supervision of a Principal Investigator. The role involves direct patient interaction, phlebotomy, pediatric experience, and community outreach responsibilities.
Key Responsibilities
Clinical Operations
Perform complex clinical procedures (ECG, spirometry, vital signs, sample collection).
Conduct phlebotomy (mandatory requirement) and handle pediatric patients.
Safeguard participant well-being and ensure adherence to safety and ethical standards.
Maintain a safe working environment per Health and Safety policies.
Act as a volunteer advocate and proactively resolve volunteer/visitor concerns.
Report deviations from normal clinical practice to senior staff.
Study Coordination
Review study protocols, CRFs, and electronic data capture systems.
Participate in study-related and project team meetings.
Prepare for study setup: label specimen containers, set up equipment, and prepare documents.
Plan logistics for clinical procedures according to study protocols.
Generate volunteer instructions and manage required supplies/equipment.
Deliver study-specific training materials and documentation.
Troubleshoot study issues and participate in daily huddles to ensure task completion.
Data & Quality Management
Perform data quality checks and resolve queries to maintain protocol adherence.
Ensure accuracy and completeness of all collected data and records.
Collaborate with study monitors and investigators to report AEs and SAEs as per protocol.
Maintain compliance with ICH-GCP and company SOPs in all study-related activities.
Volunteer Recruitment & Interaction
Recruit and screen volunteers based on eligibility criteria.
Provide study orientation to participants, explaining purpose, procedures, and timelines.
Administer and maintain custody of study drugs as per SOPs.
Qualifications
Education & Experience
High School Diploma (or equivalent).
Minimum 1 year of relevant experience in clinical research.
Prior experience in a clinical research setting preferred.
Valid certifications/licenses as required by local or state regulations.
Technical & Professional Skills
Working knowledge of clinical trial operations and GCP principles.
Understanding of study protocols, consent forms, and study schedules.
Strong clinical skills in performing required procedures.
Knowledge of medical terminology and documentation standards.
Detail-oriented with excellent organizational and problem-solving abilities.
Strong interpersonal skills to collaborate with coworkers, patients, and investigators.
Additional Notes
Phlebotomy and pediatric experience are mandatory.
This position does not offer sponsorship.
Compensation
Base Pay Range: $35.00 – $42.00 per hour
Actual pay may vary based on experience, education, skills, and location.
Additional benefits may include bonuses, incentive plans, and health/welfare programs.
About IQVIA
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and life sciences solutions. We accelerate medical innovation through data-driven insights to improve global health outcomes.
🔗 Learn more: https://jobs.iqvia.com
🌐 Equal Opportunity Employer: IQVIA does not discriminate based on race, color, religion, sex, gender identity, sexual orientation, national origin, disability, veteran status, or any other protected category.
🔗 https://jobs.iqvia.com/eoe
Application
Apply Now to join IQVIA’s mission to improve global healthcare through innovation and research excellence.
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