Senior Vice President, Technical - Clinical Regulatory Affairs

Responsibilities

Work on a variety of assignments, diverse product types for clients Creating opportunity for clients throughout the product lifecycle Sharing scientific, technical, regulatory and/or commercial expertise Leading teams of respected SMEs Meeting new situations and learning Provide mentoring and guidance to other RS employees

Requirements

MD or PhD required 15+ years experience with expert level industry or regulatory knowledge experience in Clinical Development/Clinical Trial Design, Clinical Strategy, and authoring clinical sections of regulatory applications Previous experience with a regulatory agency (such as the FDA or MHRA) as a Senior / Master Medical Review Officer, Team Lead, etc. or a related Medical role is strongly preferred Extensive Neuroscience, Rare Disease, Immunology, Endocrinology/Metabolism experience is highly preferred Ability to travel up to 20-30% domestically and/or internationally may be required for Client and/or Health Authority Meetings and Thought Leadership/Conference Attendance

Certifications & Qualifications

MD PhD

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