Providing expert communications leadership, the contract External Communications Associate Director will manage clinical regulatory writing activities, author complex documents, and drive strategic communication initiatives while working remotely. Key responsibilities Independently manage clinical regulatory writing activities across a complex portfolio of work Lead internal and external authoring teams, ensuring timely and quality delivery of clinical-regulatory documents Drive the development of the clinical Submission Communication Strategy (cSCS) and advocate for quality and efficiency in communication standards Required qualifications Master's degree in Life Sciences or a related discipline; Ph.D. is desirable Significant medical writing experience in the pharmaceutical industry or CRO Strong understanding of drug development and communication processes In-depth knowledge of technical and regulatory requirements related to the role Proven ability to advise and lead communication projects effectively
External Communications Director in workfromhome at Unknown Company
This position is listed as contract and able to be worked remotely.