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Regulatory Specialist

Job

Insight Global

Hackensack, NJ (In Person)

$66,560 Salary, Full-Time

Posted 1 day ago (Updated 6 hours ago) • Actively hiring

Expires 6/7/2026

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Job Description

Job Title:
Regulatory Specialist Company:
Hackensack Meridian Health Location:
100 First Street, Hackensack, NJ 07601
PR:
$27-$37
Duration:
6 month contract (+ extensions or conversion)
Schedule:
M-F:
9am-5:30pm
JOB DESCRIPTION
Insight Global is seeking a Regulatory Specialist with hands‑on clinical research site experience to join the Clinical Research team at Hackensack Meridian Health in Hackensack, NJ. This on‑site, 40‑hour‑per‑week contract role will support day‑to‑day site‑level regulatory operations for active clinical trials, ensuring compliance with institutional, federal, and sponsor requirements. On a daily basis, the Regulatory Specialist will prepare, submit, and manage IRB documentation including initial submissions, protocol amendments, continuing reviews, and informed consent updates; maintain complete and audit‑ready regulatory binders; track and manage essential documents within CTMS and document management systems; and serve as a primary regulatory point of contact for PIs, study teams, sponsors, CROs, and IRBs. The role also involves supporting protocol activation and ongoing study maintenance, preparing for and assisting with site audits, inspections, and monitoring visits, addressing regulatory findings through corrective and preventive actions, and managing multiple studies simultaneously in a fast‑paced clinical research environment while ensuring ongoing compliance with FDA regulations, ICH‑GCP guidelines, and institutional policies. MUST‑HAVE
REQUIREMENTS
Bachelor's degree in life sciences or a related field (Master's preferred) IRB submission and submitting by themselves Minimum 2-3 years of hands‑on clinical research site regulatory experience Direct experience with the IRB lifecycle at the site level, including; Local IRB submissions Informed consent documents Continuing reviews Protocol amendments Strong working knowledge of: IRB processes FDA regulations GCP guidelines Proficiency with CTMS and regulatory document management systems Strong organizational and communication skills Proven ability to manage multiple studies and deadlines in a fast‑paced research environment On‑site availability required (no remote or hybrid)
Pay:
$27.00 - $37.00 per hour
Benefits:
401(k) Dental insurance Health insurance Vision insurance
Work Location:
In person

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