SUMMARY

The Associate Director, Therapeutic Area Medical Lead Hematology is part of the Medical Affairs Team and represents his/her area of responsibility towards external and internal stakeholders. Owing to his/her profound understanding of the respective treatment area and extensive network the Therapeutic Area Medical Lead establishes and fosters collaborations with external partners and provides a bridge between clinical development, medical affairs and the commercial organization at a senior mastery level. He/she provides critical insights into the country medical affairs plan for the respective disease areas ensuring that it complements the company´s development plan and adheres to the highest scientific standards.

REQUIREMENTS

• MD, PharmD or PhD in life sciences
• Long standing experience in the pharmaceutical industry, extensive external network within the field of hematology
• Leadership experience is a plus
• Track record of successful cross-functional pre-launch planning and launch execution within malignant hematology, notably within the area of myeloid and lymphatic diseases
• At least 3 years experience as information officer as per §74a German Drug Law
• Experience with the planning and implementation of EAP and compassionate use requests within the field of rare diseases/hematology
• Launch expertise within the company´s key therapeutic areas (MF, DLBCL) is considered a plus
• Excellent communication skills including in complex and business-critical situations towards regulatory authorities, GBA/AMNOG hearings
• Ability to identify scientific questions and data gaps within the development program, notably those relevant for the German treatment and reimbursement landscape and to address them within the country medical affairs program
• Prior experience in a role with budget responsibility (planning, accuracy) is considered a plus
• Ability to work independently and effectively in complex, rapidly changing environments
• Sense of urgency
• Interested in new ways of thinking and innovative approaches
• Flexibility, diplomacy, and the ability to manage expectations
• Ability and willingness to travel up to 25% of working time
• Language: German, English fluent
• Proficient in Outlook/Word/Excel/PowerPoint
  Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
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• Constantly builds and maintains expertise in the assigned areas (tumor entities, products), regarding available literature, treatment options, disease environment and product data; key contact for external and internal stakeholders, including for training and all educational approaches
• Serves within his area of responsibility as the primary point of contact internally and externally notably to provide a first-level assessment for all IIR requests with regards to scientific value and fit with the company strategy
• Actively contributes to the advancement of the national development program within his/her area of responsibility
• Actively participates – whenever feasible - in medical & scientific exchanges within medical/scientific community and fosters collaborations with key external stakeholders
• Identifies scientific questions relevant to the German healthcare landscape and develops and executes a strategy to address them within the (hematology) medical affairs program to ensure the full value of our drugs is recognized by key external stakeholders
• Anticipates relevant changes in national treatment patterns (i.e. future approvals, updated guidelines) and provides timely input into the national medical affairs plan to ensure ongoing patient and scientific benefit
• Defines – in collaboration with the executive medical director – medical pre-launch and launch strategy and tactics for all hematology products and aligns cross-functionally with all relevant functions (commercial, MA) to ensure launch excellence
• Supports publication strategy within the country hematology medical affairs program to ensure that scientific results stemming from the national IIR projects are acknowledged within the scientific community in a timely manner
• Provides oversight and contributes to the preparation and delivery of high quality content and all educational and medical communication materials (e.g. planning for medical society presence, abstracts, and publications)
• Streamlines product communication, works with external and internal resources on the development of materials (for internal and field/external use) and medical event planning
• Participates in relevant cross-functional medical planning, working groups and task forces
• Ensures appropriate execution of medical content elements of the tactical plan for assigned product(s) and therapeutic area(s)
• Contributes positively to a strong culture of business integrity and ethics and embraces the Mission, Vision and Values of the organization
• Acts within compliance, regulatory and legal requirements as well as within company guidelines