Clinical Research Coordinator- Manhattan, NY (Temp to Perm)

The IMA Group; New York (NY); On-site; USD 60,000 - 65,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with employer match

Tuition reimbursement and student loan

Paid parental leave

PTO

Job summary

The IMA Group is seeking a experienced Clinical Research Coordinator for a position in Manhattan, NY. This hands-on role involves coordinating trials, interacting with sponsors and staff, and ensuring audit-ready documentation.

Candidates should have 2+ years of clinical research coordination, with phlebotomy proficiency, IM/SQ injections, and medication reconstitution experience. Bachelor's degree preferred; Master's a plus.

Qualifications

• 2+ years of clinical research coordination experience with phlebotomy proficiency.
• Experience administering IM and SQ injections.
• Experience with medication reconstitution.
• Bachelor's degree preferred; advanced degrees a plus.

Responsibilities

• Coordinate clinical trials per protocol and SOPs.
• Serve as a key point of contact with sponsors, CROs, CRAs, IRBs, and site staff.
• Support investigators and ensure accurate, audit-ready documentation (ALCOA).
• Report adverse events and safeguard study data integrity.

Skills

Phlebotomy proficiency

IM/SQ injections

Medication reconstitution

Multitasking across studies

CCRC certification a plus

Education

Bachelor's degree preferred

Associate's degree with equivalent experience considered

Master's degree a plus

Job description

Clinical Research Coordinator — Manhattan, NY

$60,000–$65,000/year

IMA Clinical Research is seeking an experienced Clinical Research Coordinator for a role in Manhattan, NY — a great opportunity to join a stable, established research site.

Why you'll like it here:

• No on-call responsibilities — predictable schedule
• Hands-on clinical role with real variety — injections, reconstitution, and full trial coordination

What you'll do:

• Coordinate clinical trials per protocol and SOPs
• Serve as a key point of contact with sponsors, CROs, CRAs, IRBs, and site staff
• Support investigators and ensure accurate, audit-ready documentation (ALCOA)
• Report adverse events and safeguard study data integrity

What you bring:

• 2+ years of clinical research coordination experience with phlebotomy proficiency
• Experience administering IM and SQ injections
• Experience with medication reconstitution
• Bachelor's degree preferred (Associate's degree with equivalent experience considered); Master's a plus
• Comfort managing multiple studies independently
• CCRC certification a plus, not required

Benefits:

• Medical, dental, and vision insurance
• PTO, paid holidays, and a floating holiday
• 401(k) with employer match
• Tuition reimbursement and student loan repayment assistance
• Paid parental leave

The IMA Group is an Aff…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.