Alzheimer's Disease International Medical Director (M/F/X)

Switzerland, Basel-City, Basel

defresrutritptzhja

• Job facts

Alzheimer's Disease International Medical Director (M/F/X)

Leads and oversees the medical strategy, associated programs, activities and team(s) for the assigned disease area within the assigned division. Works cross-functionally to develop and support the medical and scientific vision and strategies of the assigned disease area. Provides strategic direction on medical differentiation of products during product development, designs and supports clinical trials to generate medical evidence, publishes results of clinical trials and promotes and leads the exchange of medical and scientific information about disease diagnosis and disease management. Serves as spokesperson on medical, scientific and clinical matters to internal and external constituents. Selects, develops and evaluates employees to ensure the efficient operation of the function. MD is required.

Objectives and Scope of Position:

• IMD is the core PDMA role responsible for the development and execution of evidence generation strategy for the assigned product(s)/disease area (DA) based on key insights and perspectives from multiple stakeholders (HCPs, patients, nurses and payers)


• IMD provides medical/clinical expertise and input into the development of market access, brand and lifecycle strategies for the product(s)/DA


• Accountable and responsible for the benefit risk assessment of the assigned product(s) in relation to Medical Affairs evidence generation and activities  


• Stays abreast of internal and external developments, trends and other dynamics relevant for the assigned DA to maintain a fully current view and perspectives of external influences 

Summary of Main Responsibilities  Medical Strategy:

• Accountable for the evidence generation strategy planning and execution, incl. (but not limited to) identifying medical and access gaps and needs as part of the overall medical strategy  Evidence Generation Strategy:


• Drives and leads the strategy of the integrated evidence generation activities, incl. clinical studies, Investigator Initiated Studies (IIS), RWD and others 


• Accountable for the oversight of all clinical trials within medical affairs for assigned product(s)/DA, including affiliate clinical trials


• Identifies potential medical interests for line extensions according to scientific rationale and good understanding of the actual and anticipated future directions of medical practice 


• Assesses the needs and coordinates compassionate use of the assigned product(s) Patient Access: 


• In collaboration with GPMA and IMT, identifies the evidence generation needs/gaps in order to obtain and maintain patient access and integrates them into the evidence generation strategy


• Provides medical expertise and input into the market access, brand and lifecycle strategies and plans (e.g. Life Cycle Plans, Brand Plans, Launch Plans,  Comparative Benefit Risk Assessments and other relevant documents)


• Represents PDMA and provides medical expertise to the IPST and other relevant teams  External Collaborations:


• Develops, advances and maintains TAE interactions and collaborations, incl. those aimed to set up and conduct evidence generation activities


• Represents Roche in peer-to-peer interactions with external collaboration partners, including in patient-company interactions

Summary of Extended ResponsibilitiesExecution of Evidence Generation Activities:

• Accountable for evidence generation activities for a product/DA, including risk benefit assessment and medical monitoring in all medical affairs interventional studies 


• Conducts review and approval of investigator initiated studies (IIS) and supported study proposals 


• Reviews affiliate study synopses and signs off affiliate studies 


• Signs off on study concepts, synopsis and protocols of PDMA studies 


• Takes the role of Lead Scientific Responsible and acts as a member of the SMT   


• As appropriate, provides medical expertise and scientific data to support Regulatory, Drug Safety, Health Economics and  Public Policy strategy and documents  


• For established products, contributes to the comparative benefit-risk assessment and integrates the new benefit elements from clinical studies and other data sources in the overall benefit context

Medical Education and Congress Activities:

• Contributes to the medical education needs assessments  


• Accountable for the medical content of the medical education activities and publications

(applicable for Senior/Principal IMD) in collaboration with the SCD/SCL

• May present relevant data at congress events (e.g. affiliate briefings) and provide medical education to internal stakeholders


• Signs off medical education materials, Q&A and other documents for internal distribution and/or for external use (applicable for Senior/Principal IMD)


• Provides guidance to other GMT members on how to translate complex scientific/medical information into lay terms (e.g. patient materials  etc.) Promotional materials:


• Accountable for accurate and balanced medical information 


• Reviews and approves (sign off)  promotional materials  (applicable for Senior/Principal IMD) Advisory boards:


• Provides input on the advisory board plan for the assigned product(s)/DA


• Responsible for the medical scientific robustness of the information presented and for advice seeking questions 


• Responsible for aligning advisory board advice requests with all internal and external stakeholders, such as GDT, LCT and advisors, in collaboration with the ISD 


• Leads and may present the medical/scientific aspects of assigned product(s) at the advisory board meetings Budget:


• Responsible for the budget oversight of the respective area and activities in close collaboration with the GMTL and the Project Manager Compliance:


• Responsible for acting in line with legal, regulatory and company standards and codes of practice  •       Completes all required training modules as priority  Cross-functional collaboration:


• Acts as an  IBT, IMT, IPST member and may lead IMT 


• Acts as a member and/or may lead the Medical Launch Team 


• May represent GMT in LCT and GDT across all stages of life cycle, including early development  (applicable for Senior/Principal IMD)

Job levels:

• Associate IMD: Entry level. No pharmaceutical experience required. Participates mainly in execution of evidence generation strategy


• IMD: Is able to work across all aspects of the role under guidance of a more senior IMD. Contributes to the analysis of access evidence needs and provides relevant input into integrated evidence generation plan. Participates in various activities related to evidence generation, patient access and external stakeholder collaborations, as appropriate and assigned by GMTL   


• Senior IMD: Is able to work independently. May act as a brand/disease area expert. When appointed and appropriate, may represent PDMA in LCT and GDT. Fully accountable for evidence generation strategy, including access evidence plan. Anticipates the importance of new stakeholders and oversees stakeholder collaborations with regard to evidence generation strategy development


• Principal IMD: Typically leads evidence generation strategy for a complex molecule or indication.  Acts as an ambassador for the DA, both within PDMA and beyond. Is typically assigned to the most complex and strategically critical projects and/or evidence generation programs in the relevant DA. Drives innovation (incl. implementation of new methodologies, digital care solutions) and cross-functional collaborations 

Professional and Technical Requirements

• MD with relevant clinical experience (patient care decision-making) at the point of care. Specialization degree and experience in the disease area are a plus.  

Technical Competencies:

• High ethical standards Ability to demonstrate Roche Values and Leadership Commitments


• Strategic agility and decision-making ability


• Functional competencies, including but not limited to organization, prioritization and planning skills, negotiation skills, communication & presentation skills Ability to operate successfully in a matrix environment with shared accountability and responsibilities


• Ability to work across multiple cultures and countries

Experience, Skills, Knowledge

• Professional experience, both in clinical practice and within the pharmaceutical industry (preferably in medical function at global or regional/affiliate level) 


• Strong knowledge of the overall drug development process and experience in development and implementation of clinical trials Relevant clinical and scientific knowledge


• Previous experience with launch of drugs/indications is a plus  Proven expertise with a wide range of data and information (e.g. scientific, clinical and   regulatory)


• Experience in the principles of data analysis, interpretation and assessing clinical relevance 


• Experience of partnership with TAEs and external organizations is strongly preferred 


• Good understanding of business context,  incl. access evidence requirements and external value/decision-making drivers is preferred


• Fluency in written and spoken English

• Who we areAt Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
  
  Roche is an equal opportunity employer.


• Job facts
  
  
  
  • Location Switzerland, Basel-City, Basel
  
  
  • Function Medical Affairs
  
  
  • Subfunction Medical Information/Scientific Affairs
  
  
  • Schedule Full time
  
  
  • Job level Individual contributor
  
  
  • Job type Regular
  
  
  • Division Roche Pharmaceuticals
  
  
  • Posted since 2019/02/07
  
  
  • Job-ID 201901-102991
  
  


• Get in touchMr. Artur Prib


• You could also like these jobs

  International Medical/ Scientific Director (IMD/ISD), NMO

  Switzerland, Basel-City, Basel

  (Senior) International Medical Director (M/F/X)

  Switzerland, Basel-City, Basel

  Alzheimer's Disease International Medical Director (M/F/X)

  Switzerland, Basel-City, Basel