Medical Engagement Lead - Munich, Deutschland - Bristol-Myers Squibb

Bristol-Myers Squibb

Geprüftes Unternehmen

Munich, Deutschland

vor 3 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity.

Take your career farther than you thought possible.

Position Summary

The primary role of MEL is to engage in meaningful peer-to-peer scientific dialog with healthcare system National Thought Leaders (NTLs) within a defined geography.

The MEL conducts critical activities that support advancing science, educating on evolving clinical practices, transforming science into patient care, and facilitating the development of new research collaborations (including IIT and RWE).

The role collaborates with colleagues on capturing medical insights and acts as a therapeutic area resource to cross-functional partners.

Engagement with TLs should be aligned with medical strategies, and the role should provide insight back to home office to inform strategy.

This role is field-based and regional in scope.

It is anticipated that the employee will spend at least 60% of the time in the field interacting with external stakeholders, including investigators and clinical thought leaders while supporting internal stakeholders and maintaining a high level of therapeutic expertise.

Key Responsibilities

Engaging in highquality peertopeer scientific dialog with key National thought leaders in Dermatology/ Rheumatology focused on pre

- and peri-launch period.
-
Medical Strategy Advisory

Collaborates with NTLs to identify and generate insights on evolving care paradigms to inform medical strategy
Provides strategic input into materials for national medical congresses. Collects meaningful medical insights and communicates to the medical and commercial organizations to support strategy development and business decisions.

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Evidence facilitation

Facilitates scientific partnerships and research collaborations in collaboration with GDD
Provides recommendations and insights to the clinical development team on study feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with home office medical and GDO
Proactively leads BMS major evidence readouts to investigators partnering with GDD. Reactively discuss major evidence readouts with other thoughtleaders
Liaises with large key accounts to understand clinical levers and barriers to patient access in the context of clinical trials

-
Medical engagement:

Effectively collaborates and communicates with NTLs to gain insights into the clinical landscape
Engages in scientific and clinical conversation to ensure the development of a product/disease areafocused medical plan that translates into effective launch and LCM activities
Responsible for conducting evidence readouts with the most prominent institutions, e.g., Ph 3 topline data.
Engages with medical societies, PAG, and guideline discussions as appropriate.
Engage accountlevel decision makers in selected AMCs to help identify barriers and solutions to improve patient care and outcomes

Required Qualifications & Experience

MD recruited from top clinical practice and hospitalacademic centers or PhD with a very strong external profile.
Proven record of developing high impact peertopeer relationships and influence with high impact NTLs.
Strong Dermatology and/ or Rheumatology experience required:
scientific or clinical area, patient treatment trends, clinical landscape

- pharmaceutical industry, including compliance and regulatory guidelines
- clinical trial design and process
- national and regional healthcare and access environment

Working in a scientific and/or clinical research environment.
Deep understanding of TL environment and needs.

Key competencies desired

Scientific Agility

Ability to engage in a peertopeer dialog about data in a fair and balanced way
Expert knowledge of clinical practice and evolving healthcare delivery models
Ability to understand and critically appraise scientific publications
Knowledge of clinical trial design and methodology, including Good Clinical Practices and ethical, governmental, and regulatory requirements.
Understands treatment paradigms and can frame information in a convincing way that resonates with physicians
Excellent communication and presentation skills to articulate scientific and clinical data in an easytounderstand manner to help HCPs best serve their patients
Has a strong learning mindset and passion for science. Prioritizes staying current with the latest data