Summit Therapeutics

Associate Director, Regulatory Affairs

Summit Therapeutics · Remote (US)

Posted 8 days ago

or apply directly on Summit Therapeutics's site. We never take the application ourselves.

Is this posting real?

This role has been open
8 days
Summit Therapeutics's roles stay open a median of 28 days
Reposted
No
Salary listed
No
0% of Summit Therapeutics's roles list one
Ghost-job risk at Summit Therapeutics
moderate
18 stale, 3 reposted of 80 open
Hiring momentum
111 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 Summit Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Summit Therapeutics.

About this role

The Associate Director of Regulatory Affairs at Summit Therapeutics will oversee regulatory activities for clinical studies, particularly focusing on ivonescimab in oncology. Daily tasks include providing regulatory guidance, developing global regulatory strategies, managing submissions to regulatory agencies, and ensuring compliance with regulations. The role also involves liaising with health authorities and leading cross-functional teams in regulatory meetings.

Our read on this posting3.0out of 5
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 Summit Therapeutics as an employer.

What you need

  • BA/BS degree in Biotechnology, Biological Sciences, or related field
  • Minimum of 5+ years of experience in regulatory affairs
  • Global regulatory experience
  • Knowledge of US FDA and international pharmaceutical guidance and regulations
  • Strong written and oral communication skills in English
  • Strong negotiation skills and ability to work under pressure

Nice to have

  • Graduate-level degree (e.g., MS, PhD, or PharmD)
  • Knowledge of Chinese
  • Experience interacting with CROs in managing ex-US CTAs
  • Experience with electronic document management systems

What you get

  • Pay range of $168,000 — $198,000 USD
  • Potential for bonus, stock, and other variable compensation

Worth weighing

  • Remote position may require self-motivation and discipline
  • Role involves significant responsibility and pressure due to regulatory deadlines
  • No specific mention of work-life balance or flexibility in hours

Summarised from Summit Therapeutics's posting. Read the full original.

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

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