Medical/scientific Director, Oncology Blenrep

vor 2 Wochen

Zug, Schweiz GSK Vollzeit

**Site Name**: Philadelphia Walnut Street, GSK House, Switzerland - Zug, UK - London, USA - Massachusetts - Waltham, Waltham, Zug House

**Posted Date**: Feb 9 2023
- Are you interested in a leadership opportunity to drive the implementation of effective Clinical Oncology strategies for a multi-national pharmaceutical company? If so, this role may be for you _

Position Summary

Working independently, the Medical/Scientific Director is capable of fully leading designated aspects of the Medical Affairs strategic planning process and its implementation on behalf of the Global Medical Affairs Leader (GMAL) and in collaboration with her/his peers and other functions in the medical affairs team. The scope of the role therefore mirrors parts of the scope of the GMAL role, to whom she/he is accountable. This may include the following activities:

- Plays an integral role in building/optimizing the Global Medical Affairs Plan (MAP) and Integrated Evidence Plan (IEP) for the relevant asset/indication(s).
- Drives delivery of designated above-country elements of the MAP, e.g., Advisory Boards, Symposia, Educational Events.
- Partners with commercial colleagues to optimize brand strategy, campaigns and launches in the Franchise Local Operating Companies (LOCs).
- Leading and overseeing partnerships from a GMA perspective for the relevant asset/indication(s).
- Drives the development and/or approval of promotional, educational, training and other materials and responses.
- Drives the congress planning and coordination from a brand perspective, including pre
- and post-congress deliverables
- Drives the scientific training coordination and execution from a brand perspective, including material development and/or approval
- Delivers the evidence needs for that asset on behalf of the GMAL in partnership with R&D:

- Drives the efficient working of the Integrated Evidence Team; ensuring insights from Franchise LOCs are integrated appropriately to inform the IEP.
- Reviews local GSK-sponsored and Investigator Sponsored Study (ISS) proposals from Franchise LOCs to assess their scientific merit and strategic need, liaising with R&D experts.
- Accountable for the development of assigned Franchise study protocols.
- Drives excellence in Scientific Engagement (SE) with key stakeholders (HCPs, Patients, Payors and Regulators) to gain a deep understanding of customer needs.
- Deputizes regularly for the GMAL as required.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

- Gathers medical insights from the Franchise Local Operating Companies (LOCs) and external stakeholders (HCP’s, Patients, Payors and Regulators) to shape the integrated evidence strategy and global medical affairs plans and strategy.
- Leads medical lead research activities including Expanded Access Programs
- Leads Advisory Board design and discussion ensuring compliance with SE governance and documentation requirements
- Leads Symposia and other Educational Activities design and discussion ensuring compliance with SE governance and documentation requirements
- Inputs to the design and delivery of phase IIIb/IV studies and EAPs, including post-approval commitments, coordinating with relevant R&D technical experts.
- Responsible for the review of local GSK-sponsored and Investigator Sponsored Study (ISS) proposals from Franchise LOCs to assess their scientific merit and strategic need, liaising with R&D, safety, biostats, and other experts.
- Facilitates preparation for the Brand Planning processes, ensuring compliance with timelines and mandated global templates to ensure consistency across Franchises/Franchise LOCs.
- Plays an integral role in the development and approval of brand strategy, and promotional campaigns and materials.
- Develops/reviews publications/abstracts/posters related to the product, key competitors, and relevant disease area(s). Ensures the Data Dissemination Plan (DDP) is maintained.
- Supports the GMAL in communicating effectively the clinical and market access data for their asset to the Franchise LOCs; ensures a robust understanding of risk: benefit.
- Enhances local tactical plans and shares best practices to support Launch Excellence.
- Supports the GMAL in providing medical governance oversight for the asset, including management of product-related issues with potential impact on patient safety, and medical budget management.
- Responsible for leading and overseeing partnerships from a GMA perspective for the relevant asset/indication(s).
- Drives excellence in Scientific Engagement (SE) with key stakeholders (HCPs, Patients, Payors and Regulators) to gain a deep understanding of customer needs.
- High level of responsibility for successful delivery of critical projects and processes.
- Responsible for building and driving the Global Medical Affairs strategy and IEP for the asset/indication(s), on behalf of the GMAL.
- Building credibil

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