or apply directly on Seaport Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 10 days Seaport Therapeutics's roles stay open a median of 68 days
- Reposted
- No
- Salary listed
- No 78% of Seaport Therapeutics's roles list one
- Ghost-job risk at Seaport Therapeutics
- high 7 stale, 0 reposted of 9 open
- Hiring momentum
- 11 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-24
Measured from postings appearing on and disappearing from Seaport Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Seaport Therapeutics.
About this role
The Associate Director of Regulatory Affairs at Seaport Therapeutics will lead regulatory project teams and manage submission activities for neuropsychiatric medicines. This role involves providing strategic regulatory guidance, ensuring compliance, and collaborating with cross-functional teams to integrate regulatory requirements throughout the development lifecycle. The candidate will also engage with global health authorities and contribute to the preparation of IND/CTA and NDA/MAA submissions.
- benefits
- 1/5
- freshness
- 5/5
- 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 Seaport Therapeutics as an employer.
What you need
- Bachelor’s degree required
- 7+ years in global regulatory affairs
- Expertise in early development (Pre-IND/IND) and late-phase strategy for CNS therapies
- Experience leading IND/CTA and/or NDA/MAA submissions
- Proven success in leading Pre-IND or INTERACT meetings for psychiatry/neurology programs
- Designing Phase II PoC studies with validated endpoints
Nice to have
- Advanced degree in a scientific discipline preferred
What you get
- Expected salary range is $180,000-$205,000
- Encouragement of open conversations about compensation
Worth weighing
- Onsite work is preferred 4 days per week
- Role involves a significant amount of regulatory compliance work which may be high-pressure
- Focus on CNS therapies may limit exposure to other therapeutic areas
Summarised from Seaport Therapeutics's posting. Read the full original.
Listed by Seaport Therapeutics on their greenhouse job board, last confirmed open on 2026-10-24. PitchMeAI is not the employer.