MMS, an award-winning clinical research organization, is seeking a Nonclinical Document Writer to join their remote team in the UK. The successful candidate will have a BS in pharmacology or a related field, with at least 2 years of regulatory nonclinical writing experience. Responsibilities include developing and managing complex nonclinical documents, collaborating with cross-functional teams, and ensuring compliance with regulatory guidelines. Join an innovative company that values employee contributions and offers a supportive work environment.
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