Clinical Research Coordinator (CRC) – Phlebotomy Required in Warren, NJ
The IMA Group, Trenton, NJ, United States
Clinical Research Coordinator (CRC) – Phlebotomy Required
Warren, NJ | $50K–$65K + Benefits
IMA Clinical Research is hiring an experienced Clinical Research Coordinator (CRC) to support industry-sponsored clinical trials at our Warren, NJ site.
This is a hands-on role ideal for someone with active investigational product (IP) trial experience who can independently manage studies and perform patient-facing procedures.
What You’ll Do
Coordinate clinical trials from startup through closeout
Execute protocols in compliance with FDA & GCP guidelines
Perform phlebotomy, vitals, and study-related procedures
Communicate with sponsors, CROs, and site teams
Maintain accurate, audit-ready documentation
Report AEs/SAEs per protocol
What You Need
2+ years CRC experience (required)
Industry-sponsored trial experience with active IP (required)
Phlebotomy skills (required)
Bachelor’s degree required
CCRC preferred
Why IMA?
Strong pipeline of active studies
Growth-focused environment
Full benefits + 401k match + PTO
The IMA Group is an Affirmative Action/Equal Opportunity Employer
Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
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Warren, NJ | $50K–$65K + Benefits
IMA Clinical Research is hiring an experienced Clinical Research Coordinator (CRC) to support industry-sponsored clinical trials at our Warren, NJ site.
This is a hands-on role ideal for someone with active investigational product (IP) trial experience who can independently manage studies and perform patient-facing procedures.
What You’ll Do
Coordinate clinical trials from startup through closeout
Execute protocols in compliance with FDA & GCP guidelines
Perform phlebotomy, vitals, and study-related procedures
Communicate with sponsors, CROs, and site teams
Maintain accurate, audit-ready documentation
Report AEs/SAEs per protocol
What You Need
2+ years CRC experience (required)
Industry-sponsored trial experience with active IP (required)
Phlebotomy skills (required)
Bachelor’s degree required
CCRC preferred
Why IMA?
Strong pipeline of active studies
Growth-focused environment
Full benefits + 401k match + PTO
The IMA Group is an Affirmative Action/Equal Opportunity Employer
Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
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