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- The Medical Advisor is accountable to initiate, develop and deliver medical and scientific input and activities for an assigned product in the Oncology therapeutic Area. Responsible for ensuring medical strategy and tactics are in place for the assigned product accountabilities include ution of an overall medical strategy for the individual products in alignment with regional/global TA objectives. Responsible for engaging with Key External Experts in Oncology TA, and working closely with key internal stakeholders, including the brand teams across the affiliate to achieve business objectives for the affiliate.
- Essential Job Responsibilities: List 10 or fewer primary duties and responsibilities for this position in order of importance and time spent. Include supervisory responsibilities. Focus on responsibilities rather than projects. Avoid being vague or listing many minor duties.
- 1. Medical Affairs Strategy & Tactics
- a. Coordinate timely medical input of tactics into the Core Medical Plan (CMP) tools for planning, updating the CMP tracker and uting the CMP within timelines and budget in the affiliate.
- b. Execute medical activities such as internal and external scientific product presentations and participating or leading advisory boards to gain further insight for Medical Affairs strategies and tactics.
- c. Provide medical input to commercial activities for the product brand teams including the planning, preparation and approval of
- i. Strategic business plans
- ii.Product training to marketing and sales colleagues in the affiliate.
- d. Provide external medical and business environment perspective and TA knowledge to the cross-functional stakeholders in the affiliate.
- 2. Data Generation for HCPs and Payers
- a. Partner closely with the Health Economics and Outcomes Research (HEOR) and Market Access to provide insight on local access strategies and challenges and close data gaps
- b. Partner with market access in reimbursement or listing discussions with payers/hospitals as needed
- c. Lead creation of Company Initiated Trial(CIT) concept with internal stakeholders including the clinical operations team.
- d. Support the Country(ies) head and regional reviewers in reviewing as well as appropriate documentation of Investigator Sponsored Research/ Grants for general research/ Grants for Medical Education/ Sponsorship for Research & Education
- 3. Data Communication and Medical Education
- a. Provide medical / scientific education and training to internal stakeholders on marketed products and compounds in development
- b. Strategically manage the development of local Non-Promotional Medical Materials in alignment with TA objectives, including, but not limited to slide presentations and posters / manuscripts
- c. Identify and engage key external customers (KEEs) in in-depth medical and scientific product or disease area discussions / scientific exchange, and presentations to communicate the value of Astellas products in a fair and balanced way in accordance with Astellas values/code of conduct as well as applicable local regulations
- d. Develop, maintain, engage with key external experts (KEEs), healthcare professionals, healthcare organizations funding bodies and other entities to engage and communicate the value of Astellas products in a fair and balanced way accordance with Astellas values/code of conduct as well as applicable local regulations
- 4. Collaboration with Commercial
- a. Planning and preparation of new product or new TA entry and Leading and driving strategic collaboration
- b. Champion a collaborative mindset to ensure full alignment with key stakeholders cross-functionally
- c. Review and approve promotional materials complying with local and applicable internal/external regulations and/or policies.
- d Provide scientific /medical support to Marketing, Market Access, Business Intelligence (advice, reports, recommendations, etc.).
- e Coordinate in uting medical-scientific activities in product launches: disease area presentations, expert meetings.
- f Participating as a therapeutic area/product expert in internal meetings of the company and provide medical-scientific support for external meetings in a fair and balanced manner (post-approval symposia)
- g. Provide consistent training on therapeutic area and products to the colleagues (including commercial) in the Country.
- 5. Field Medical Activities
- An office-based hybrid professional with scientific and therapeutic-area expertise in disease state management, brands, emerging therapies, and the competitive landscape
- Responsible for identifying accessing and effectively engaging with 15-30 (depending on the product/disease characteristics and size of the TA business) active and potential KEEs aligned with the respective therapeutic area strategies that foster scientific exchange and collaboration.
- 6. Mentors and coaches others within Field Medical Affair
- 7. Legal/Compliance Skills
- a. Ensures all Country medical affairs activities are in compliance with all applicable Astellas policies, external regulations and ethical standards
- b. Manages expectations of both internal and external stakeholders regarding what Medical Affairs can and cannot do based on solid understanding of company, regulatory and legal boundaries by maintaining up-to-date knowledge of regulatory guidelines, local country code of practice and Astellas quality documents to ensure adherence in all areas as appropriate.
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