# Executive Medical Director, Specialty and Pipeline

**Company**: Bayer
**Work arrangement**: remote
**Experience**: executive
**Job type**: full-time
**Salary**: $248,000 to $372,000
**Category**: Medical
**Industry**: Pharmaceuticals

**Apply**: https://talent.bayer.com/careers/job/562949976864247
**Canonical**: https://yubhub.co/jobs/job_83bd1570-20c

## Description

At Bayer, we're seeking an Executive Medical Director, Specialty and Pipeline to oversee the development and execution of high-quality medical strategy for our pipeline portfolio.

As a critical member of the US Medical Affairs team, you will be responsible for providing scientific leadership, external engagement, and cross-functional influence to advance evidence generation, medical education, and development of medical affairs strategy to support commercialization strategic plans of the portfolio.

Key responsibilities include:

- Overseeing US medical affairs strategy and contributions into the Bayer pipeline portfolio in collaboration with medical directors and in alignment with the VP of Specialty and Pipeline TA.

- Providing input, appropriate to the Phase of development of a product to ensure US perspective and needs are incorporated into development strategy.

- Active participation and effective collaboration with global teams to assure the efficient and expedient conduct of clinical development programs, aligning them with strategic priorities that support appropriate US direction of the Life Cycle Management strategy.

- Working collaboratively with US New Product Commercialization, Market Access and US regulatory teams to provide expert medical input into strategic plans.

- Serving as a member of Product Team and/or Clinical Strategy Team leadership of multiple assets in different therapeutic areas.

- Supporting development and execution of the US medical strategy, offering critical inputs during design and throughout the end-to-end execution of programs, in alignment with senior medical leadership.

- Collaborating cross-functionally with Global Evidence Generation, Clinical Development, Regulatory, Commercial and other medical affairs partners to develop and implement the Integrated Evidence Plans to improve the value proposition for the portfolio.

- Contributing to publication planning, data interpretation, and scientific dissemination in the US.

- Providing medical scientific input for brand and program documents, including integrated disease area plans, medical information documents, drug safety reporting documents, etc, while ensuring design and execution of all medical activities are according to internal and external compliance guidelines.

- Monitoring and understanding implications of evolving competitor landscape to inform medical strategy.

- Supporting completion of annual New Drug Application (NDA) reports for respective brands through evaluation of clinical data and literature and provide US Medical Affairs input in the preparation of key medical documents for INDs and NDAs.

Additionally, you will:

- Develop and guide local Thought Leader (TL) engagement strategy, together with cross-functional partners.

- Serve as the US medical expert engaging thought leaders, academic institutions, medical societies, and patient advocacy groups to advance scientific leadership and collaboration.

- Lead and support advisory boards, including agenda development, faculty engagement and synthesis of insights to help inform medical strategy.

- Represent US Medical Affairs at major congresses, symposia and scientific forums.

To be successful in this role, you will need:

- An M.D. or D.O. degree.

- Agility and ability to flex into different therapeutic areas.

- Clinically relevant work experience or independent research experience or equivalent or experience in a pharmaceutical related industry.

- Experience working in or deep understanding of in-hospital consideration in US healthcare delivery.

- Deep understanding of clinical trial design, analysis and interpretation as well as the principles of observational studies and health economics/ outcomes research.

- Robust understanding of regulatory and market access considerations and triangulating those to implications on clinical trial design and clinical care delivery.

- Proven ability for strategic planning along with operations skill and experience related to clinical research involving both single and multiple centers.

- Strong ability to quickly build meaningful and trusting relationships, both internally and externally to the organization.

- Understanding of the drug development process over different stages.

- Strong ability to connect and collaborate across different functions and background, both internally and externally to the organization.

- Innate ability to lead others without formal authority, with demonstrated experience guiding teams from design to implementation of strategic initiatives.

- Excellent communication skills, both verbal and in written.

- Willingness and ability to travel as business dictates, both for internal and external functions.

Preferred qualifications include:

- Board certification or board eligibility in cardiovascular, neurology, critical care medicine.

- 7 years work experience in the pharmaceutical sector in Medical Affairs, Clinical Development or related positions.

- Experience in the field of medical support of a product portfolio across multiple therapeutic areas.

- Experience in leading and participating in teams across cultures and geographies, prior experience in global medical launch planning activities.

## Skills

### Required
- M.D. or D.O. degree
- Agility and ability to flex into different therapeutic areas
- Clinically relevant work experience or independent research experience or equivalent or experience in a pharmaceutical related industry
- Experience working in or deep understanding of in-hospital consideration in US healthcare delivery
- Deep understanding of clinical trial design, analysis and interpretation as well as the principles of observational studies and health economics/ outcomes research
- Robust understanding of regulatory and market access considerations and triangulating those to implications on clinical trial design and clinical care delivery
- Proven ability for strategic planning along with operations skill and experience related to clinical research involving both single and multiple centers
- Strong ability to quickly build meaningful and trusting relationships, both internally and externally to the organization
- Understanding of the drug development process over different stages
- Strong ability to connect and collaborate across different functions and background, both internally and externally to the organization
- Innate ability to lead others without formal authority, with demonstrated experience guiding teams from design to implementation of strategic initiatives
- Excellent communication skills, both verbal and in written
- Willingness and ability to travel as business dictates, both for internal and external functions

### Nice to have
- Board certification or board eligibility in cardiovascular, neurology, critical care medicine
- 7 years work experience in the pharmaceutical sector in Medical Affairs, Clinical Development or related positions
- Experience in the field of medical support of a product portfolio across multiple therapeutic areas
- Experience in leading and participating in teams across cultures and geographies, prior experience in global medical launch planning activities