Senior Medical Director, Clinical Development- POVE

Job DescriptionGeneral Summary:The Senior Medical Director will define the clinical development strategy of povetacicept in primary membranous nephropathy, work with cross-functional multidisciplinary teams to define overall asset strategy as well as clinical trials strategy, design and execution, and may serve as the Medical Lead for clinical trials that will be conducted with these compounds. Key Duties and Responsibilities:Defines a clinical development strategy and prepare the clinical development plans, in conjunction with other relevant functional areasParticipates in the development of study protocols, statistical analysis plans, investigator's brochures, and other key study documents in conjunction with other line functions and with minimal guidanceLeads the Project Team, and works with cross-functional team members to define a project strategy and ensure execution against approved strategyParticipates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of INDs and CTAs, safety reports, responses to regulatory authorities, clinical study reports, and other documents as appropriateInterfaces with regulatory authorities as appropriateMonitors and/or oversees medical monitoring of clinical studiesParticipates in business development and strategic planning activitiesActs as liaison between clinical development and other internal groups at Vertex for assigned studiesProvides medical and development leadership for cross-functional teamsServes on cross-functional study teams for assigned trials, working with other team members to achieve efficient, high-quality study execution, and data analysisRepresents Vertex to outside medical personal in the development of clinical protocols and study conductAs a people manager within the organization, may have financial accountabilities and human resource responsibilities for assigned staff.Knowledge and Skills:Global clinical research experience, and experience interacting with regulatory authorities is highly desiredAbility to work collaboratively in a fast-paced, team-based matrix environmentAbility to work independently to resolve challengesEnterprise-wide thinking and ability to work in ambiguityAbility to ensure the completeness of team workExcellent oral and written communication skillsBoard certification/eligibility in a specialty is highly desired.Education and Experience:MD, DO or equivalent ex-US medical degreeBoard certification/eligibility in a specialty is highly desiredTypically requires 12 years Pharmaceutical/Biotech industry experience, including time managing clinical trials and clinical development programs, or the equivalent combination of education and experienceSupervisory experience required#LI-JM1#LI-HybridPay Range:$280,600 - $420,800Disclosure 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 EligibleFlex 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 select2.    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-HybridCompany InformationVertex 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.comSummaryLocation: Boston, MAType: Full time