Clinical Research Coordinator

1 years

$35.00 – $42.00

New York

10 Sept. 8, 2025

Job Description

Job Type: Part 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

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

How to Apply:

Apply Now at IQVIA Careers

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Clinical Research Coordinator

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