Emea Medical Affairs Director Hematology
il y a 2 semaines
Johnson & Johnson is currently seeking an EMEA Medical Affairs Director Hematology to join our EMEA Strategy & Operations organisation.
**Responsibilities**:
To develop the EMEA Medical Strategy and the EMEA Medical Affairs Product Plan (MAP Plan) for Ciltacabtagene Autoleucel and Talquetamab in line with Global strategy and in alignment with the Integrated Brand Value Team (IBVT) strategy, taking into account both weighted needs of the EMEA countries and feedback from the external scientific communities/thought leaders.
To represent EMEA MAF which includes shaping the brand strategy.
To lead the functional networks as required, and to ensure effective communications between the key regional and global groups. To act as the Medical Affairs expert and drive a unified EMEA Medical voice.
To represent the unified EMEA MAF voice at the GMAT.
To drive the implementation of the activities outlined in the EMEA Medical Affairs Product strategies and Plan across EMEA in close cooperation with other EMEA functions (EMEA Medical Affairs Program Lead [EMPL], Scientific Knowledge Management [SKM], Medical Education Scientific Relations [MESR], Regulatory Affairs, Strategic Marketing, Health Economics)
To oversee the EMEA Medical Affairs budget for pan-EMEA activities for those assigned product(s) for which the EMAD is accountable.
CORE ACTIVITIES:
EMEA Medical Affairs Product Leadership
- Act as the EMEA MA expert and drive the strategy for a specific product or group of products:
- articulate the consolidated medical voice for EMEA
- represent EMEA voice at regional and global teams (IBVT, GMAT, lifecycle teams)
- develop and maintain detailed knowledge in products, market trends, competitor activities etc.
- Build-up/maintain network with external thought leaders
- provide expertise to EMEA functions (Medical, Commercial, Health Economics, Regulatory Affairs etc.) and functional network in the countries
- Oversee the EMEA Medical Affairs budget for pan-EMEA activities for assigned product(s) for which EMAD is accountable.
- To represent EMEA MAF for specific product or group of products, which includes shaping the brand strategy and providing input into the development of the EMEA plan ensuring alignment with the strategy
- Lead the EMEA Medical Affairs Product Team (EMAP team: EMEA Medical Programme Lead (EMPLs), MESR (Medical Education Scientific Relations, SKM (Scientific Knowledge Management) and the Medical Affairs functional network to deliver EMEA MA Strategy and Plan:
- Work with the EMAP Team to gather input for the EMEA Medical Affairs Product Plan(s) for designated product(s) according to the EMAP Team charter
- Draft the EMEA Medical Affairs Product Plan for allocated product(s) and drive the review and approval process with the EMAP team, EMEA Therapeutic Area Team (ETAT), the EMEA Medical Affairs Leadership Team (EMALT) and IBVT
- Work with the EMAP Team to proactively identify and provide medical input into opportunities for new indications or lifecycle extensions for allocated product(s)
- Work with the EMAP Team to develop approaches to support successful market access for allocated product(s) in partnership with Health Economics, the CDT (Compound Development Team) and lifecycle management teams
- Leverage product(s) expertise, medical and market insight to shape and direct implementation of product(s) strategies and plans
- Work with the EMAP Team and Medical Affairs functional network to drive the implementation of the Strategy and Plan
- Ensure effective and regular communications between Global, Regional and local MA teams
- Being a member of the GMAT: and CDTs
- To represent the unified EMEA voice,
- To shape global MA Strategy,
- To ensure input in Compound Development Team (CDT), including input into phase II/ III designs, and country and site selection and on life cycle management strategy
- To provide input into publications plan
- and into Medical Educations plan/activities into EMEA soil
Accountable for line managing EMEA Medical advisor:
- Allocation of responsibilities for product ownership and other activities
- Objective setting
- Performance management and performance evaluation
- Coaching and feedback outside of the formal performance management processes
- Ensure that appropriate training (e.g. internal seminars) in core MAP Team, Medical Affairs, functional skills, Good Clinical Practice (GCP) and required SOPs is undertaken
External Relationships
Maintain and leverage relationships with investigators, EMEA thought leaders and patient groups to gain input into the development of the product strategy and to specific protocols
As core MAP Team lead, ensure regular communications between EMEA and MA Functional Network to help minimise duplication of advocacy and access programmes across countries, and facilitate co-ordination between EMEA Medical Affairs, CDT, Strategic Marketing, Health Economics and individual countries
Product Safety and Regulatory Requirements
As pe
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