Clinical Research Coordinator — Temp-to-Perm, No On-Call

The IMA Group; New Jersey; On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Insurance

PTO & holidays

401(k) match

Tuition reimbursement

Parental leave

Job summary

The IMA Group is hiring an experienced Clinical Research Coordinator for a temp-to-perm role in Warren, NJ—a stable, established research site. You will coordinate Phase II–IV clinical trials per protocol, serve as a key contact with sponsors, CROs, CRAs, IRBs and site staff, and support investigators while ensuring audit-ready documentation (ALCOA).

You will report adverse events and safeguard study data integrity.

Qualifications

• 2+ years of clinical research coordination experience.
• Experience vaccinating patients required.
• Bachelor's degree preferred (Associate's degree with equivalent experience considered); Master's a plus.
• RN preferred.
• Comfort managing multiple studies independently.
• CCRC certification a plus, not required.
• 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.

Responsibilities

• Coordinate clinical trials per protocol and SOPs (Phase II–IV).
• 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

vaccinating patients

multitask studies independently

ALCOA documentation

Education

Bachelor's degree preferred

Associate's degree with equivalent experience considered

RN preferred

Job description

The IMA Group is hiring an experienced Clinical Research Coordinator for a temp-to-perm role in Warren, NJ—a stable, established research site. You will coordinate Phase II–IV clinical trials per protocol, serve as a key contact with sponsors, CROs, CRAs, IRBs and site staff, and support investigators while ensuring audit-ready documentation (ALCOA).

You will report adverse events and safeguard study data integrity.