Director, Regulatory Strategy (29074) Contract

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.

The ideal candidate will be an independent, strategic thinker who will have the ability to make strategic recommendations.  Experience with market product, labeling, new drug development and working with the FDA required.

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
• Provides regulatory leadership to the GRA functional team(s) or projects with moderate resource requirements or complexity
•  

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

$115-$125/hr

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors