GMA Map Lead Job in New Jersey (NJ), Research and Development Career, Full Time Jobs in Novartis Pharmaceuticals
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GMA Map Lead job in East Hanover

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Novartis Pharmaceuticals jobs
New Jersey (NJ), East Hanover
Job Code:  245780BR
Employer:  Novartis Pharmaceuticals
Category:  Research and Development
Job Type:  Full Time

Location
Country:  United States
State:  New Jersey (NJ)
City:  East Hanover
Map: 
09/05/2018

Description
The GMA MAP Lead is responsible for coordinating and providing oversight and transparency on Managed Access Programs (MAPs) across Oncology Medical Affairs (OMA). The GMA MAP Lead will track KPIs and Metrics of the medical and operational management of the MAP portfolio across OMA. This role requires an in depth understanding of the MAP process including associated budgeting.

Major Accountabilities

•Provide an oversight on Managed Access Programs (MAPs) across Oncology Global Medical Affairs
•Identify operational efficiencies and best practices amongst the MAP portfolio within current GOP
•Act as Subject Matter Expert for all MAPs in OMA: Act as the central point of escalation for Franchise Teams for all MAP-related issues and potential deviations
•Identify requirement of preparation of new MAP Treatment Plan and coordinate corresponding activities with Franchise Team
•Receive and track all Cohort MAP/IPR requests
•Liaise with Medical Responsible on MAP request approval/rejection and track decision as well as overall MAP strategy (inclusion/exclusion of disease types)
•Partner with Global Clinical Supply to support MAP drug supply process as needed
•Ensure annual MAP Treatment Plan updates are prepared as applicable
•Drive the operational excellence for the MAP portfolio across OMA through KPI and metrics; Identify trends on the outcomes of metrics and KPIs and develop mitigation plans as required.
•Maintain budget oversight on all global MAP activities
•Provide MAP process and budget updates, as applicable, to GMA and OMA Leadership
•Participate in cross-functional MAP Governance Board and MAP related initiatives
•Participate in co-authoring/ review of MAP related SOPs/GOPs as applicable

Key Performance Indicators

1.Timely, efficient and compliant approval/rejection of MAPs/IPRs within Oncology Medical Affairs
2.Strong oversight of the OMA MAP portfolio-highlighted through metric and KPI reporting
3.Coordination of regular update of product MAP strategies based on evolving science in collaboration with GMDs/GGMDs
4.Effective management of potential risks and challenges for all activities within remit
Education:
Degree or equivalent education in life science/healthcare preferred

Experience:

•≥5 years of pharmaceutical/CRO clinical research experience, preferably in global matrix environment

•≥2 years MAP experience required

•Proven ability to work independently

•Established knowledge of clinical development process, GCP and clinical project management. Novartis experience in these areas is preferred.

•Strong interpersonal, problem-solving, negotiation and conflict resolution skills

•Ability to influence without authority in highly matrixed organization

•Organizational awareness, including experience working cross-functionally and in global teams

•Experience in developing effective working relationships with internal and external stakeholders

•Proactive team player with an ability to act in a forward-thinking and collaborative manner

•Ability to proactively identify and propose practical operational solutions to address forecasted and unforecasted business issues

•Compliance oriented
ref: (245780BR)
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