IQVIA · 1 week ago
Clinical Research Coordinator - Troy, NY
Troy, NY
Part-time
Onsite
Entry Level
$35/hr - $42/hr
1+ years expIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. The Clinical Research Coordinator will perform complex clinical procedures, coordinate research studies, and ensure participant safety while maintaining compliance with best practices and protocols.
AnalyticsHealth CareLife Science
No H1B
Responsibilities
Perform a variety of complex clinical procedures on subjects, including but not limited to ECG, sample collection (including spirometry), and vital signs
Phlebotomy is required; pediatric experience is preferred
Participate in community outreach as part of recruitment efforts
Coordinate clinical research studies conducted by a supervising Principal Investigator
Maintain and update skills, training, and knowledge of current best nursing practices and clinical research topics
Safeguard the well-being of subjects and uphold high standards:
Maintain a safe environment in accordance with Health and Safety policies
Act as a volunteer advocate and address concerns proactively
Assist staff in clinical coordinator practices and care delivery
Report any deviation from normal practice to senior staff
Support Study Conduct By
Reviewing study protocols, CRFs, and electronic data capture systems
Participating in project meetings as needed
Performing clinical set-up and preparation for studies, including labeling specimen tubes, setting up equipment, and preparing documents
Planning logistical activities for procedures per protocol
Generating volunteer instructions and preparing study-specific training materials
Troubleshooting study issues and participating in daily huddles to ensure task execution
Assisting with data quality checks and query resolution to ensure protocol adherence
Recruiting and screening volunteers based on pre-determined criteria
Orienting volunteers to the study and site, including timelines and procedures
Administering and maintaining custody of study drugs per SOPs
Collecting, recording, and reporting clinical data accurately in CRFs
Collaborating with investigators on adverse events and serious adverse events reporting
Cooperating with study monitors and following ICH GCP guidelines for all activities
Qualification
Required
High School Diploma and at least 1 year of relevant clinical research experience (or equivalent education and experience)
Applicable certifications and licenses as required by company, country, state, and/or regulatory bodies
Working knowledge of clinical trials and Good Clinical Practices (GCP)
In-depth knowledge of protocol-specific procedures, consent forms, and study schedules
Skill in performing required clinical procedures and familiarity with medical terminology
Strong attention to detail and ability to maintain effective working relationships with coworkers, managers, patients, physicians, and clients
Preferred
At least 1 year in a clinical research setting preferred
Pediatric experience is preferred
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
10001+ employees
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
Recent News
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