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Iterative Health

Clinical Regulatory Specialist

Iterative Health · NYC, Cambridge or Southlake HQ

Posted about a month ago

or apply directly on Iterative Health's site. We never take the application ourselves.

Is this posting real?

This role has been open
30 days
Iterative Health's roles stay open a median of 45 days
Reposted
No
Salary listed
No
0% of Iterative Health's roles list one
Ghost-job risk at Iterative Health
high
29 stale, 1 reposted of 55 open
Hiring momentum
88 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Iterative Health's own greenhouse board since 2026-08-03. Full hiring picture for Iterative Health.

About this role

As a Clinical Regulatory Specialist at Iterative Health, you will support the execution of Phase 2–4 clinical trials by managing regulatory activities throughout the study lifecycle. Your responsibilities will include preparing and maintaining essential regulatory documents, coordinating IRB submissions, and ensuring compliance with regulatory requirements. You will collaborate with clinical research sites and various stakeholders to facilitate study progress and maintain inspection-ready documentation.

Our read on this posting3.4out of 5
benefits
5/5
freshness
4/5
career value
4/5
role clarity
4/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Iterative Health as an employer.

What you need

  • 2+ years of relevant experience in clinical research, regulatory affairs, clinical operations, or a related field supporting industry-sponsored clinical trials
  • Experience supporting Phase 2–4 sponsor-initiated clinical trials, ideally in a site-facing regulatory capacity
  • Previous experience as a Clinical Research Coordinator (CRC), Regulatory Coordinator/Specialist, or in another site-facing clinical research role with responsibility for regulatory activities
  • Working knowledge of Good Clinical Practice (GCP), applicable FDA requirements, IRB processes, and clinical research Standard Operating Procedures (SOPs)
  • Experience preparing and maintaining essential regulatory documents and supporting IRB submissions throughout the study lifecycle
  • Strong organizational, time-management, and prioritization skills

Nice to have

  • Experience with a Clinical Trial Management System (CTMS), electronic regulatory platform, eSource, or other clinical research technology

What you get

  • Hybrid work environment with in-office collaboration two days per week
  • Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered
  • Mental health and wellness support through Spring Health
  • Health HSA or FSA options, and commuter FSA contributions
  • Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years
  • 401(k) program with a company match of up to 3%

Worth weighing

  • Fast-paced and highly iterative growth environment may require adaptability
  • No specific salary information provided
  • Role involves managing multiple studies and priorities, which may be demanding

Summarised from Iterative Health's posting. Read the full original.

Listed by Iterative Health on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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