Global Regulatory CMC Lead, Small Molecules

A biotechnology firm is seeking an Associate Director, Regulatory CMC to develop and implement global regulatory strategies for small molecule therapeutics. Responsibilities include managing regulatory submissions, supporting clinical trials, and ensuring compliance with CMC activities. Candidates should have a Bachelor's degree in a life science field and at least 8 years of experience in CMC Regulatory Affairs. The position requires strong interpersonal and organizational skills in a fast-paced environment.
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