Senior Manager, Regulatory Compliance

Job Description General Summary: The Regulatory Compliance Senior Manager works to provide compliance oversight, guidance and direction to all relevant Regulatory Affairs functions, key stakeholders and leadership teams primarily through process development and refinement. The incumbent will be responsible for championing these processes throughout the teams, working with Senior Management to prioritize process work, identifying authors and adapting to an evolving global landscape. This incumbent will help define compliance standards via policies and procedures, elevate compliance matters to internal stakeholders and deliver compliance training and communications as necessary. Key Duties and Responsibilities: Provides compliance oversight, guidance and direction to all relevant employees, key stakeholders and leadership teams. Partners with cross-functional teams to collaborate, negotiate and drive fact- and risk-based decision making. Assists teams in identifying areas where compliance input and escalation is required and ensures consistency in the application of criteria across the Company. Serves on various cross-functional teams and forums as appropriate to identify and assess risks and develop solutions to mitigate risk. Elevates compliance matters to internal stakeholders. Collaborates with Global Regulatory Affairs stakeholders to ensure compliance with policies and regulatory requirements. Delivers compliance training and communications as necessary. Supports the Quality System as pertains to GRA, and its applicable subsystems as assigned; oversight of quality systems and compliance. Acts as the Global Regulatory Affairs Lead for quality framework for Standard Operating Procedures and Work Instructions; liaison between stakeholders and Quality Document Control. Identifies procedural gaps and areas for improvements and works with Senior Management to prioritize process work and identify authors. Knowledge and Skills: In-depth conceptual knowledge and experience in interpretation of regulations, guidelines, and precedents related to Quality Management Systems and global regulatory and development activities. Strong communication and interpersonal skills to explain difficult information and build alignment. Experience in cross-functional process development. Results-oriented problem solver. Exhibits strong organizational and project management skills necessary to perform complex tasks independently and work on multiple projects simultaneously. Education and Experience: Bachelor's degree in a scientific or allied health field. Typically requires 6 years of experience including cross-functional experience in Clinical Development, Biostatistics, Regulatory Affairs and/or Quality Assurance at a pharmaceutical or biotech company, or the equivalent combination of education and experience. Flex Designation: Hybrid-Eligible Or On-Site Eligible Flex Eligibility Status: In this Hybrid-Eligible role, you can choose to be designated as: 1.

Hybrid : work remotely up to two days per week;

or select 2.

On-Site : work five days per week on-site with ad hoc flexibility. Company Information: Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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