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Iterative Health

Senior Clinical Regulatory Specialist

Iterative Health · NYC, Cambridge or Southlake HQ

Posted 28 days ago

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

Is this posting real?

This role has been open
28 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 Senior Clinical Regulatory Specialist at Iterative Health, you will oversee regulatory activities for Phase 2–4 clinical trials, ensuring compliance throughout the study lifecycle. Your role involves collaborating with various stakeholders, managing regulatory submissions, and providing guidance to research sites. You will also drive process improvements and mentor less experienced team members, all while maintaining a focus on regulatory excellence and compliance.

Our read on this posting3.6out of 5
benefits
5/5
freshness
4/5
career value
4/5
role clarity
5/5
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

  • 4+ years of relevant experience in clinical research, clinical regulatory, and/or research operations supporting industry-sponsored clinical trials
  • Strong 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 clinical research role with significant responsibility for regulatory activities
  • Strong working knowledge of Good Clinical Practice (GCP), applicable FDA regulations and guidance, IRB processes, and clinical research SOPs
  • Demonstrated experience independently managing regulatory activities across multiple studies and/or research sites
  • Experience reviewing regulatory documentation and submissions for quality, completeness, and compliance

Nice to have

  • Experience mentoring, training, or providing guidance to less experienced team members
  • 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 by Iterative Health
  • Mental health and wellness support through Spring Health
  • Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health
  • 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% (up to $3,000 annually)

Worth weighing

  • No salary listed
  • Fast-paced environment may require strong adaptability
  • Role involves significant independent management of complex regulatory activities

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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