Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical company seeks a Regulatory Affairs Senior/Consultant in Hartford, CT. This role involves leading regulatory CMC strategy for innovative peptide and oligonucleotide therapeutics. The ideal candidate has 4–7 years of relevant experience, strong analytical skills, and a solid understanding of regulatory requirements. Responsibilities include managing submission activities and compliance across teams. Candidates located in EST are preferred, with opportunities for exceptional candidates in other US or Canadian time zones.
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