Johnson & Johnson Careers
EMEA Medical Affairs Evidence Dissemination Manager (MEDM)
Requisition ID: 00001EV3
OVERALL PURPOSE OF JOB:
Purpose of the role is to focus on our Evidence Dissemination strategy (Publication planning, Public Relationship campaigns, use of Social Media, Communication through MSL network, …)
To shape our EMEA Medical Affairs Evidence Dissemination Ambition & Framework to maximize the reach & impact of our evidence generated Value Stories with our target audiences
To advise the organization of market trends & drive innovation in the area of Evidence Dissemination and leverage Competitive intelligence insights to help develop & improve our Competitive Advantage
To help the EMAP teams develop their Evidence Dissemination plans by supporting their discussions and challenging their plans
To develop & maintain our Operational Framework (processes & tools) for Evidence Dissemination to define performance, compliance and quality metrics and support internal stakeholders to more easily and effectively present all available evidence
To be responsible for our Evidence Dissemination performance, compliance and quality metrics, training programs and act as Subject Matter Expert.
Shaping EMEA MAF Evidence Dissemination Strategy
Collaborate with EMPD, EMPMs, ETALs, Communications, Government Affairs, R&D and Senior MAF management to:
Define our department Ambition for Evidence Dissemination
Agree a change management plan
Agree clear quantitative & qualitative goals and ED strategies across all TAs, with the objective to maximize reach & impact of our Company Evidence.
During Integrated Evidence Generation Planning, review and discuss the level of investment for Evidence Dissemination as well as Evidence Generation in line with respective Brand Ambition and position in its lifecycle (pre-launch & launch vs post-launch stage)
Connect with internal functions interfaced with our target audience (e.g. Communications, Gov. Affairs, Patient Engagement) to discuss our EMEA MAF Evidence Dissemination Strategy and ensure alignment
On an annual basis, develop & share a status overview on the outcomes of our Evidence Dissemination Plans, the evolution of our framework and any Challenges & Opportunities
Internal & External Benchmarking / Innovation
Network and maintain relationships with internal and external stakeholders to ensure awareness of the latest market trends & innovation
Organize benchmarking & mapping of Competition approach regarding Evidence Dissemination
Propose, pilot & lead the development of new initiatives aimed at improving reach, impact or efficiency.
Product/TA Evidence Dissemination Plans
Partner with EMAP teams to support, contribute to and challenge their Evidence Dissemination Plans and ensure they are investing proper time & resources in Evidence Dissemination Planning
Monitor the implementation of Evidence Dissemination plans by EMAP teams and ensure plans are revisited and adapted on a regular basis
Evidence Dissemination Framework
Develop and maintain Evidence Dissemination processes & tools (PubShare, PubStrat, etc…) and interface with relevant internal functions (Communications, Global MAF, Patient Engagement, etc…)
Define and manage efficient methods by which evidence can be disseminated to key internal stakeholders to enable them to more easily and effectively present all available evidence
In partnership with key stakeholders (e.g. procurement, contracting, legal,…), facilitate the set-up & implementation of Evidence Dissemination activities to ensure we have all process, vendor pre-selection, contracting in place in line with our Company Quality, HCC & Legal requirements
Organize Best Practices Sharing / Lessons Learned across all EMAP teams & relevant MAF functions
Performance, Compliance, Quality & Training
Develop, maintain & improve system & tools to measure the reach & impact of our Evidence Dissemination activities
Define and manage Compliance & Quality metrics related to our Evidence Dissemination Activities
Act as Subject Matter Expert / Champion on all matters related to Evidence Dissemination
Organise and deliver necessary training for our EMEA MAF organization on Evidence Dissemination Framework & Tool(s).
- Excellent knowledge of scientific publication management, scientific communication, use of social media, Public Relationship.
Good understanding of study design & execution and related regulations (GCP, European Directives,).
Highly innovative with the ability to drive multiple projects within a complex and changing environment.
Excellent interpersonal and interdependent partnering skills.
Strong and demonstrable communication and influencing skills that can impact at a Global and regional level
Ability to work effectively in a matrix environment, with multi-cultural, virtual teams.
Master degree or higher in a pharmaceutical-related or Communication subject
Minimum 8 years of experience of industry experience in Scientific Communication.
Good understanding of the varying clinical research practices (Phase I to III clinical trials, RWE Post Marketing Data collection activities, Investigator Initiated Activities, ...) and related activities across EMEA
- Fluency in English language and excellent written English skills essential.
- Fluency in additional EMEA languages an advantage
The role is Central Europe based. The role holder will be expected to be based in their current country of residence as long as easy access to travel/ transportation and local hosting is available in a Janssen office.
The role involves EMEA and International travel (10 %).
Europe/Middle East/Africa, Europe/Middle East/Africa-Switzerland, Europe/Middle East/Africa-Italy, Europe/Middle East/Africa-Germany, Europe/Middle East/Africa-Spain, Europe/Middle East/Africa-France, Europe/Middle East/Africa-United Kingdom
Janssen Pharmaceutica N.V. (7555)