Senior Regulatory Submissions Specialist
Listed on 2026-10-30
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Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Summit Therapeutics Inc. seeks a Senior Specialist, Regulatory Operations to lead hands-on preparation and publishing of regulatory submissions, including eCTD packages, for INDs, CTAs, and health authority responses.
The role requires 4+ years in Regulatory Operations, strong knowledge of FDA/ICH standards, and experience with Veeva RIM or Promo Mats. Excellent document formatting and cross-functional collaboration are essential.
For the Senior Regulatory Submissions Specialist position at Open Krill, we are reviewing applications now.
The position is based in United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 122..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Regulatory Submissions Specialist role in the description above.
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