A biopharmaceutical consulting firm is seeking a Senior CMC Regulatory Affairs Consultant to guide regulatory strategies for innovative therapies in a fully remote capacity. The role involves collaborating with interdisciplinary teams and ensuring compliance with global standards. Candidates should possess 4-7 years' experience in peptide and oligonucleotide synthesis, and a relevant degree in chemistry or related fields. This opportunity emphasizes professional development and impactful projects on patient health.
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