A leading recruitment platform is seeking a Senior CMC Regulatory Affairs Consultant to support a global biopharmaceutical client. This fully remote role involves guiding regulatory strategies for innovative peptide and oligonucleotide therapies, requiring 4-7 years of relevant experience. Key responsibilities include preparing regulatory submissions, leading interactions with health authorities, and collaborating with multidisciplinary teams. The position offers flexible hours and the opportunity to impact patient health significantly.
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