Executive Medical Director- Nephrology

Vertex Pharmaceuticals Incorporated; Boston (MA); Hybrid; USD 320,000 - 480,000; Full time

Benefits offered by this job

Hybrid-Eligible

On-Site Eligible

Job summary

Vertex is seeking an Executive Medical Director, Clinical Development to provide high-level input on clinical development strategies for povetacicept renal programs, in collaboration with Medical Affairs, Regulatory, Global Patient Safety, Clinical Operations, Exploratory Development, Commercial, Pharmaceutical Development, Research, Business Development and Marketing.

You will initiate and lead innovative approaches to clinical development, oversee study design, monitor safety, and partner with

Qualifications

• MD, DO or equivalent ex-US medical degree.
• 15 years pharmaceutical industry experience, including time managing clinical trials and/or clinical development program(s).
• 7 years of management experience.

Responsibilities

• Provide clinical development recommendations to project teams, including optimizing study design and conduct for efficiency and effectiveness.
• Oversee medical monitoring of clinical studies.
• Interface with international regulatory authorities in support of development objectives.
• Review study protocols and Investigator Brochures; evaluate safety data.
• Ensure compliance with ICH-GCP and other regulatory requirements.
• May have personnel management responsibilities for assigned staff.

Skills

Leadership skills

Communication

Regulatory knowledge

Strategic thinking

People management

Education

MD/DO or equivalent medical degree

Job description

Job Description

General Summary:

The Executive Medical Director, Clinical Development will provide high-level input on clinical development strategies to povetacicept renal programs, in conjunction with other relevant functional area leaders in Medical Affairs, Regulatory, Global Patient Safety, Clinical Operations, Exploratory Development, Commercial, Pharmaceutical Development, Research, Business Development, and Marketing. Initiate and lead innovative approaches to clinical development.

Key Duties and Responsibilities:

• Broad and comprehensive understanding of the drug development process
• Well-respected authority in the external clinical development community
• Provide clinical development recommendations to project teams, including optimizing study design and conduct for efficiency and effectiveness.
• Participate in planning for worldwide clinical development activities
• Provide guidance to multi-disciplinary development teams
• Review study protocols
• Review Investigator Brochures
• Review and evaluate study subject exemptions
• Oversee medical monitoring of clinical studies
• Evaluate adverse events and overall safety profile
• Participate in data reviews
• Interface with international regulatory authorities, as appropriate, in support of the development objectives for the compound or program
• Ensure compliance with Vertex Standard Operating Procedures, International Conference on Harmonization, Good Clinical Practice, and other national and international regulatory requirements
• 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
• Possesses a comprehensive understanding of applicable US and EU regulatory requirements and of the drug development process
• Possesses a working knowledge of biostatistics, data management, clinical operations and clinical pharmacokinetic scientific and technical processes
• Experience in filing and defending US INDs and/or NDAs and/or their international equivalents
• Enterprise-wide thinking and ability to work in ambiguity, including being hands on in order to ensure the work that needs to be done by the team gets done; other duties as required or assigned
• Ability to work and lead collaboratively in a challenging fast-paced, team-based matrix environment
• Ability to work independently to resolve challenges and conflicts
• Excellent oral and written communication
• Excellent leadership skills
• Board certification/eligibility in a medical specialty desired

Education and Experience:

• MD, DO or equivalent ex-US medical degree
• 15 years pharmaceutical industry experience, including time managing clinical trials and/or clinical development program(s), or the equivalent combination of education and experience
• 7 years of management experience

#LI-JM1

At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.

Pay Range:

$320,000 - $480,000

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 a 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 [e-mail]