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Summit Therapeutics

Associate Director, Risk Based Quality Management Lead

Summit Therapeutics · Princeton, New Jersey, United States

Posted about 3 months ago

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

Is this posting real?

This role has been open
77 days
Summit Therapeutics's roles stay open a median of 64 days
Reposted
No
Salary listed
No
0% of Summit Therapeutics's roles list one
Ghost-job risk at Summit Therapeutics
high
78 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
2026-10-23

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, Risk Based Monitoring (RBQM Lead) is responsible for overseeing the operational execution of risk-based monitoring activities across clinical studies at Summit Therapeutics. This role involves collaborating with various teams to identify, evaluate, and mitigate risks throughout the clinical trial lifecycle, ensuring participant safety and data integrity. The RBQM Lead will also develop risk management plans, monitor key risk indicators, and facilitate risk review meetings to support effective study conduct.

Our read on this posting2.2out of 5
benefits
1/5
freshness
1/5
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

  • Bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical-related areas
  • 10+ years of clinical operations experience in sponsor pharmaceutical or biotechnology organizations
  • 7+ years of direct RBQM, centralized monitoring, risk-based monitoring, clinical quality, or study management experience
  • Experience supporting global Phase II and/or Phase III clinical trials
  • Experience conducting risk assessments; developing and managing KRIs and QTLs; and facilitating risk review meetings
  • Demonstrated ability to interpret complex scientific, clinical, and operational data to identify quality and compliance risks and support centralized trial monitoring

What you get

  • Pay range of $174,000 — $204,000 USD
  • Total compensation package may include bonus, stock, benefits and/or other applicable variable compensation.

Worth weighing

  • Role involves significant responsibility in risk management, which may be stressful depending on study outcomes.
  • No specific mention of remote work or flexible hours, which may be a consideration for work-life balance.
  • The position requires extensive experience in clinical operations, which may limit opportunities for less experienced candidates.

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

Listed by Summit Therapeutics on their greenhouse job board, last confirmed open on 2026-10-23. PitchMeAI is not the employer.

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