Clinical Research Coordinator - NYC Trials, Stable Schedule

IMA Clinical Research, Inc.; New York, Northern (NY, KY); Hybrid; USD 60,000 - 65,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

PTO, paid holidays, and a floating</n>

401(k) with employer match

Tuition reimbursement and student loan

Paid parental leave

Job summary

IMA Clinical Research, Inc. seeks an experienced Clinical Research Coordinator for a Manhattan, NY role. Join a stable, established research site with a predictable schedule and a hands-on clinical environment.

You will coordinate trials per protocol, liaise with sponsors, CROs, CRAs and IRBs, and support investigators with audit-ready documentation. The position values multitasking across studies and allows growth in a dynamic clinical setting.

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; Associate's degree with equivalent experience considered; Master's a plus.
• Comfort managing multiple studies independently.
• CCRC certification a plus, not required

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

Clinical coordination

Phlebotomy

Injections

Medication reconstitution

ALCOA documentation

Multi-study management

Education

Bachelor's degree

Associate's degree with relevant experience

Master's degree

Job description

IMA Clinical Research, Inc. seeks an experienced Clinical Research Coordinator for a Manhattan, NY role. Join a stable, established research site with a predictable schedule and a hands-on clinical environment.

You will coordinate trials per protocol, liaise with sponsors, CROs, CRAs and IRBs, and support investigators with audit-ready documentation. The position values multitasking across studies and allows growth in a dynamic clinical setting.