Regulatory Strategy Manager
Vertex Pharmaceuticals Incorporated, Boston, Massachusetts, us, 02298
Job Description
General Summary
The Regulatory Strategy Manager will be responsible for regulatory support for development programs or marketed products. The Regulatory Strategy Manager will contribute to the development of US regional or global regulatory strategies for development and commercialization of program(s) within the portfolio. This role requires a good understanding of regulatory affairs frameworks, the drug development process, and related concepts.
Key Duties and Responsibilities
Contributes to the development and implementation of regulatory strategy for assigned region as a member of the global regulatory affairs functional team
Develops proficiency in regional and global regulatory skills
Supports global regulatory strategy under guidance of the Global Regulatory Lead
Responsible for regulatory communications with local health authority; under supervision, may lead regulatory interactions with the health authority
Identifies regulatory requirements for development and approval pathways for assigned region
Under supervision, manages the process for preparation, submission, and approval of regulatory applications within assigned region
Provides technical regulatory input for key product development or registration documents
Works to ensure compliance of regulatory submissions with current regulations and guidance
Reviews regulatory intelligence and guidance information to continuously support regulatory strategy in assigned region
Knowledge and Skills
Good knowledge of regional regulatory affairs frameworks
Understanding of requirements and processes to maintain a product on the market; reporting and surveillance
Understanding of drug development and related concepts, such as clinical trial design, statistics, and clinical pharmacology
Ability to assess and understand complex scientific information, regulatory precedent, competitive intelligence, and regulatory guidelines
Strong problem‑solving skills
Strong written and verbal communication skills to exchange complex information with others in complex situations
Ability to work effectively within a team environment
Ability to plan, prioritize, and contribute to work and projects in a systematic and efficient manner
Education and Experience
Bachelor's degree in Biology, Chemistry, or other related discipline
Typically requires 4 years of relevant pharmaceutical or biotech industry experience or the equivalent combination of education and experience
Pay Range $124,000 - $186,000
Disclosure Statement The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market‑leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week‑long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
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.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI‑Hybrid
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.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com
#J-18808-Ljbffr
Key Duties and Responsibilities
Contributes to the development and implementation of regulatory strategy for assigned region as a member of the global regulatory affairs functional team
Develops proficiency in regional and global regulatory skills
Supports global regulatory strategy under guidance of the Global Regulatory Lead
Responsible for regulatory communications with local health authority; under supervision, may lead regulatory interactions with the health authority
Identifies regulatory requirements for development and approval pathways for assigned region
Under supervision, manages the process for preparation, submission, and approval of regulatory applications within assigned region
Provides technical regulatory input for key product development or registration documents
Works to ensure compliance of regulatory submissions with current regulations and guidance
Reviews regulatory intelligence and guidance information to continuously support regulatory strategy in assigned region
Knowledge and Skills
Good knowledge of regional regulatory affairs frameworks
Understanding of requirements and processes to maintain a product on the market; reporting and surveillance
Understanding of drug development and related concepts, such as clinical trial design, statistics, and clinical pharmacology
Ability to assess and understand complex scientific information, regulatory precedent, competitive intelligence, and regulatory guidelines
Strong problem‑solving skills
Strong written and verbal communication skills to exchange complex information with others in complex situations
Ability to work effectively within a team environment
Ability to plan, prioritize, and contribute to work and projects in a systematic and efficient manner
Education and Experience
Bachelor's degree in Biology, Chemistry, or other related discipline
Typically requires 4 years of relevant pharmaceutical or biotech industry experience or the equivalent combination of education and experience
Pay Range $124,000 - $186,000
Disclosure Statement The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market‑leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week‑long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
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.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI‑Hybrid
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.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com
#J-18808-Ljbffr