Senior Medical Director, Clinical Development- POVE

Vertex Pharmaceuticals; Boston (MA); On-site; USD 280,600 - 420,800; Full time

Benefits offered by this job

Annual bonus

401(k) matching

Generous paid time off

Educational assistance programs

Job summary

Vertex Pharmaceuticals in Boston is seeking a Senior Medical Director for Clinical Development. The successful candidate will define and lead the clinical strategy for povetacicept in primary membranous nephropathy, collaborating with multidisciplinary teams for efficient trial execution and regulatory submissions.

Applicants should have extensive experience in the pharmaceutical or biotech sectors, possess an MD or equivalent, and demonstrate leadership skills. This position offers competitive compensation and comprehensive benefits, with options for hybrid work.

Qualifications

• Typically requires 12 years Pharmaceutical/Biotech industry experience.
• Supervisory experience required.
• Experience managing clinical trials and development programs.

Responsibilities

• Define the clinical development strategy for povetacicept.
• Participate in the development of study protocols and regulatory documents.
• Lead the Project Team and cross-functional team members.

Skills

Global clinical research experience

Regulatory authority interaction

Excellent oral and written communication skills

Ability to work independently

Education

MD, DO or equivalent ex-US medical degree

Board certification/eligibility in a specialty

Job description

## Senior Medical Director, Clinical Development- POVEApplylocations: Boston, MAtime type: Full timeposted on: Posted Todayjob requisition id: REQ-29331**Job Description****General 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 areas* Participates 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 guidance* Leads the Project Team, and works with cross-functional team members to define a project strategy and ensure execution against approved strategy* Participates 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 appropriate* Interfaces with regulatory authorities as appropriate* Monitors and/or oversees medical monitoring of clinical studies* Participates in business development and strategic planning activities* Acts as liaison between clinical development and other internal groups at Vertex for assigned studies* Provides medical and development leadership for cross-functional teams* Serves on cross-functional study teams for assigned trials, working with other team members to achieve efficient, high-quality study execution, and data analysis* Represents Vertex to outside medical personal in the development of clinical protocols and study conduct* As 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 desired* Ability to work collaboratively in a fast-paced, team-based matrix environment* Ability to work independently to resolve challenges* Enterprise-wide thinking and ability to work in ambiguity* Ability to ensure the completeness of team work* Excellent oral and written communication skills* Board certification/eligibility in a specialty is highly desired.**Education and Experience:*** MD, DO or equivalent ex-US medical degree* Board certification/eligibility in a specialty is highly desired* Typically requires 12 years Pharmaceutical/Biotech industry experience, including time managing clinical trials and clinical development programs, or the equivalent combination of education and experience* Supervisory experience required#LI-JM1#LI-Hybrid**Pay Range:**$280,600 - $420,800**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.