Senior Regulatory Submissions Specialist — eCTD & FDA/ICH
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Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Job Description & How to Apply Below
Summit Therapeutics Inc. in the United States is seeking a Regulatory Operations professional to manage end-to-end eCTD submissions and regulatory records.
You will publish, QC, and track submissions to health authorities, while maintaining Veeva RIM systems and supporting cross-functional teams. The ideal candidate has a life sciences degree with 4+ years of Regulatory Operations experience, strong expertise in FDA/ICH standards, and proficiency in Word, Acrobat, and eCTD processes.
This role, Senior Regulatory Submissions Specialist — eCTD & FDA/ICH at Summit Therapeutics Inc., could be your next move.
The position is based in United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).