Director, Regulatory Affair Strategic

General Summary: The Regulatory Strategy Director will be responsible for the development and implementation of innovative global/regional regulatory strategies for assigned projects within the Vertex portfolio. This position will play a major role in shaping cohesive regulatory strategy for assigned program(s) and ensuring effective integration of broad regulatory ideas/tactics supporting program strategy. This roles assignments may be global, regional or local depending on the position and assigned region. This role will understand and translate regulatory, scientific, operational and business knowledge into effective implementation plans and strategy. Key Duties and Responsibilities:

• Leads the development of regulatory strategy for assigned projects/regions in development (from first-in-human to post
• marketing application stage) outlined in Global Regulatory Strategy Documents•
• Represents GRA on core development functional teams, project teams, and collaborate with regional leaders and teams to
• ensure unified regulatory input into clinical programs and commercial strategy•
• Addresses complex issues, providing innovative regulatory solutions and guidance to cross-functional teams and align
• communication to and from cross-functional teams, GRA functional team and GRA leadership•
• Anticipates global regulatory changes and develops proactive strategy accordingly•
• Shapes the regulatory strategy for regulatory submission documents and Health Authority communications•
• Counsels and advises GRA leadership on status of global Regulatory Affairs strategies and tactics, procedures and practices•
• Ensures the global regulatory strategy for a given project is consistent with the business objectives and is compliant with
• current regulations and guidance•
• Manages project plans and timelines to ensure all projects are appropriately prioritized and key goals are met on time•
• Contributes to the continuous improvement of existing department processes and strategies, providing recommendations in
• area of expertise

Knowledge and Skills:

• Experienced in Regulatory Affairs strategy in assigned geographic region, including direct interactions with a variety of
• stakeholders•
• Advanced technical skill in regulatory affairs science including knowledge of regulatory frameworks and external
• environments. Advanced knowledge of global/regional/local regulatory legislation, laws, procedure and guidance for
• pharmaceutical development of medicines for human use.•
• Proficient knowledge of the research and development, preclinical and clinical requirements related to drug development,
• registration, and maintenance of human pharmaceuticals•
• Proficiency in analyzing and interpreting data, protocols, safety reporting, labeling and other activities related to the phases of
• drug development for assigned products.•
• Advanced skill in creating and assessing proposals to regulatory authorities on regulatory paths and clinical plans, guiding
• development teams with recommendations for changes/refinements based on ongoing regulatory outcomes throughout
• development, and in leading productive health authority interactions, including well organized preparation of cross functional
• teams.•
• Actively uses expertise to develop others by providing coaching, guidance and mentoring.•
• A strong collaborative partner with cross functional colleagues with the ability to build consensus through the ability to present
• a clear and compelling case for ideas•
• Demonstrates excellent communication skills with ability to impact and influence the decisions of a team•

Education and Experience:

• Bachelor's degree in Biology, Chemistry, or other related discipline•
• Typically requires 10 years of relevant pharmaceutical or biotech industry experience within regulatory affairs, or the
• equivalent combination of education and experience•

Pay: $90.27 - $100.00 per hour Application Question(s):

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