Clinical Research Coordinator – Part-Time (Troy, New York)
Location: Troy, New York
Employment Type: Part-Time (16 hours per week)
Work Model: On-Site
Requisition ID: R1503635
Experience Level: 1+ Year in Clinical Research
Additional Locations Available
Position Overview
IQVIA is seeking a dedicated Clinical Research Coordinator (CRC) to support on-site clinical trial activities in Troy, New York. This part-time role offers the opportunity to contribute to high-quality research while performing essential clinical procedures and supporting study operations. Pediatric phlebotomy experience and community outreach involvement are important components of this position.
The ideal candidate brings hands-on clinical skills, strong organizational abilities, and a solid understanding of Good Clinical Practice (GCP) guidelines.
Key Responsibilities
Clinical & Participant Care
Perform clinical procedures including phlebotomy (required), pediatric blood draws, ECGs, spirometry, and vital signs.
Safeguard subject safety and maintain compliance with health and safety policies.
Act as a patient advocate and address participant concerns promptly.
Support registered and unregistered clinical staff in delivering high-quality care.
Report deviations and safety concerns to senior staff immediately.
Study Coordination & Documentation
Coordinate clinical research studies under the direction of the Principal Investigator.
Review study protocols, CRFs, and electronic data capture tools.
Conduct study setup, equipment preparation, and labeling of sample collection materials.
Manage logistical planning and procedural workflows according to protocol requirements.
Support volunteer recruitment, screening, orientation, and informed consent processes.
Ensure accurate collection, documentation, and reporting of clinical data and findings.
Administer and manage study drug per site SOPs.
Participate in data quality checks, query resolution, and monitoring visits.
Follow ICH-GCP standards in all study-related tasks.
Operational & Training Support
Prepare and deliver study-specific training documents and records.
Maintain updated knowledge of clinical procedures, nursing practices, and research regulations.
Identify required supplies and equipment, ensuring readiness for each study.
Work collaboratively with investigators, monitors, and project teams to ensure high operational standards.
Participate in daily huddles and team meetings to ensure smooth study execution.
Qualifications & Experience
Minimum Education: High School Diploma or equivalent.
Experience Required:
Minimum 1 year of relevant clinical research experience.
Pediatric phlebotomy experience required.
At least 1 year of experience in a clinical research environment preferred.
Technical Knowledge:
Working knowledge of clinical trials and Good Clinical Practices (GCP).
Familiarity with study protocols, SOPs, informed consent, and study schedules.
Ability to perform essential clinical procedures accurately.
Knowledge of medical terminology.
Core Skills:
Strong attention to detail and documentation accuracy.
Ability to collaborate effectively with physicians, patients, study teams, and site staff.
Excellent communication and interpersonal skills.
Other Requirements:
Certifications and licenses as required by state or regulatory bodies.
Sponsorship not available for this position.
Compensation
Hourly Pay Range: $35.00 – $42.00
Actual compensation is based on experience, location, qualifications, and schedule. Additional incentives and benefits may apply.
About IQVIA
IQVIA is a global leader in clinical research, healthcare intelligence, and advanced data analytics. The organization enables smarter decision-making and accelerates the development of innovative medical treatments that improve patient outcomes worldwide.
IQVIA is an equal opportunity employer. All qualified applicants will be considered without regard to legally protected characteristics.
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