Job Title:
Clinical Research Coordinator
Location:
Troy, New York
Office-based / On-site
Work Schedule:
Part-time
Scheduled Weekly Hours: 24
Work Set-Up: On-site
Job ID:
R1503635
Compensation:
Hourly Pay Range: $35.00 – $42.00
Actual pay may vary based on:
Experience, education, and skills
Location
Full-time vs. part-time status
May also be eligible for:
Incentive plans or bonuses
Health and welfare benefits
Key Responsibilities:
Clinical & Patient Care
Perform complex clinical procedures (e.g., ECGs, spirometry, vitals, sample collection)
Conduct phlebotomy (including pediatrics)
Community outreach participation
Ensure a safe environment in accordance with health & safety standards
Act as a volunteer advocate
Assist both registered and unregistered staff in coordinating volunteer care
Report deviations or safety concerns to senior staff
Study Support & Coordination
Coordinate research studies under the supervision of the principal investigator
Review study protocols, CRFs, and other documents
Participate in project and daily team meetings/huddles
Set up clinical environments, equipment, and documentation for studies
Generate volunteer instructions and manage supplies
Plan and execute study procedures per protocol
Support volunteer recruitment and screening
Administer informed consent and orient volunteers to the study
Ensure correct administration and custody of study drugs
Data & Compliance
Collect, record, and report clinical data in CRFs
Resolve data queries and ensure protocol adherence
Collaborate with investigators on reporting adverse events
Participate in monitoring visits with study monitors
Follow ICH GCP guidelines and site SOPs
Qualifications:
Minimum Requirements:
High School Diploma (or equivalent)
1+ year of relevant clinical research experience
Certifications and licenses as required by state, country, and regulatory bodies
Preferred:
Experience working in a clinical research setting
Pediatric experience and community outreach familiarity
Skills & Knowledge:
Working knowledge of:
Clinical trials and GCP (Good Clinical Practice)
Protocols, consent forms, and study schedules
Medical terminology
Strong attention to detail
Ability to work effectively with diverse teams, patients, and stakeholders
Competence in performing required clinical procedures
Additional Information:
Sponsorship is not available for this position
Applicable tags:
#LI-CES #LI-DNP #LI-HCP #ONSITE
About IQVIA:
IQVIA is a global leader in clinical research, healthcare analytics, and life sciences consulting. The company connects data, technology, and expertise to accelerate medical innovation and improve patient outcomes.
Learn more: https://jobs.iqvia.com
EEO Statement: https://jobs.iqvia.com/eoe
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