EMEA Senior Medical Advisor/Medical Education Lead Cardiovascular

OverviewAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob FunctionJob Function: Medical Affairs GroupJob Sub Function: Medical Affairs – MDJob Category: People LeaderAll Job Posting Locations: Beerse, Antwerp, Belgium, Beirut, Lebanon, Breda, Netherlands, Budapest, Hungary, Espoo, Uusimaa, Finland, Issy-les-Moulineaux, France, Madrid, Spain, Milano, Italy, NEUSS, Germany, Oslo, Norway, Pefki, Attiki, Greece, Porto Salvo, Portugal, Prague, Czechia, Warsaw, Masovian, Poland, Wien, Austria, Zagreb, Grad Zagreb, CroatiaMAIN ACTIVITIES/TASKSEMEA Medical Affairs Product Team Core MembershipTo act as a EMEA MA expert, shape and input into the strategy for a specific product or group of products:Represent EMEA voice towards internal and external stakeholdersDevelop and maintain detailed knowledge in products, market trends, competitor activities etc.Build up/maintain network with external thought leadersTo provide expertise to, as well as plan and execute the Medical Affairs Functional NetworkTo provide expertise to Operating Company functions (CVTs, Medical, Commercial, HEMAR Regulatory Affairs etc.)To provide key information for the region and expertise to Global functions (GCSO and R&D)To have a pro-active role in the EMEA Medical Affairs Product Team (EMAP team: EMEA Medical Program Lead (EMPL) and the Medical Affairs functional network) to provide input into and support the implementation of the EMEA MA Strategy and Plan:Work with the EMAP Team to SHAPE and gather insights and input for the EMEA Medical Affairs Product Plan(s) for designated product(s) according to the EMAP Team charterWork with the EMAP Team and Medical Affairs functional network to drive the implementation of the Strategy and PlanWork with the EMAP Team and Medical Affairs functional network to drive Medical Education Strategy and PlanAlongside the EDTL, take the lead on building the Launch Readiness PlanSupport effective and regular communications between EMAPT and local MA teams, including regular communications to help minimise duplication of advocacy and access programs across countries, and facilitate co-ordination between EMEA Medical Affairs, Marketing, HEMAR, Diagnostics teams and individual countriesProvide help designing and input into local publications planProvide input into Medical Education plans/activities in EMEA countriesProvide scientific input/shape strategy into Diagnostics, Biomarker strategy and Devices if applicable.Support operating companies in developing, aligning, and implementing their product strategies and tactical plans.To generate the right examples of real IMPACT for the patients and for the business.Be pro-active and empowered to assess and address opportunities and challenges with limited EDTL oversightExternal RelationshipsTo create, build up and nurture a trusted collaboration with the external scientific community in order to facilitate a continuous communication and transfer of knowledge between the company, thought leaders and a wider group of physicians and customers. To be considered as scientific expert by external leading specialists.To leverage relationships with investigators, EMEA thought leaders and patient groups to gain input into the development of the product strategy and to specific protocols.To transform those relationships into tangible projects/outcomes adding value to patients and businessStudy Planning and ExecutionTo build the MAF study Plan from strategy to execution in collaboration with the MAF team and integrating feedback from other internal stakeholders.Alongside EDTL, lead the collaboration with OpCo Medical Affairs to evaluate Investigator Initiated Study (IIS) proposals for scientific soundness and whether those are in alignment with the medical strategyWork with and support the EMPL and MADU in the oversight of EG activities.To act as Study Responsible Physician (when the Medical Advisor is a qualified medical doctor) or Study Responsible ScientistPublicationsTo help build and support the development and implementation of the EMEA MA publication plan at regional and/or local level.Support efforts that ensure that J&J guidelines for publication of studies are followed, and that all MA studies (local and EMEA) are published in accordance with J&J policy. Ensure EMEA messages relating to allocated product(s) (including core medical education materials, abstracts, medical informationmaterials, marketing materials etc.) accurately reflect scientific data and are fully compliant with applicable regulations.Medical EducationFor pan-EMEA Medical Education activities, shape Medical Education programs concept, review the program proposals and final program outline and support the review of scientific Medical Education materials in collaboration with SKL, rehearsals with speakers etc.Other Activities as RequiredProvide input to EMEA business development initiatives for allocated product(s). When requested Partner with the late lifecycle management group to provide proactive medical input for lifecycle extension opportunities as appropriateLiaise with R&D functions as needed and appropriate (eg pure substances requests, PK data requests etc)ComplianceEnsure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOP’s (Standard Operating Procedures) are met and appropriately managed when planning projects, developing materials, executing projects and contracting vendors.Ensure HCC and legal requirements are fully understood, appropriately managed and complied with when planning projects, developing materials, executing projects and contracting vendorsOTHER FEATURES OF THE JOBMay foster and manage complex collaborations with alliance partners, academic institutions, and external stakeholders to co-develop and implement innovative medical solutions that address unmet patient needsESSENTIAL KNOWLEDGE & SKILLSDeep knowledge of atrial fibrillation and/or stroke and a proven network of external experts.Good knowledge of all products within TAIn-depth knowledge and hands-on experience of clinical trial design and study data analysisGood knowledge of EU CTD and GCP requirementsGood knowledge of study execution, Global Medical Safety and regulatory affairsHighly customer and market place focused with an awareness of the importance of business resultsInnovative with the ability to coordinate and drive a complex and changing environmentStrategic vision: identifying and prioritizing insights, understanding the medical environment and adaption, shaping MAF plans, identifying needs, personalization of messages, active participation, anticipating needs.Ability to lead towards big picture thinking with attention to detailsAbility to work effectively in a matrix environment and to drive prioritizationAbility to influence internal and external stakeholders.Ability to work under minimal supervision and to lead full programs or projectsCapable of working in multi-cultural, virtual teamsVery strong and demonstrable communication and influencing skills that can impact at a Local, Regional and Global levelAwareness of, and adherence to, Johnson & Johnson Credo values, policies and SOPsFluency in English language requiredFluency in additional EMEA languages an advantageEXPERIENCEAdvanced scientific or medical degree4+ years experience in an area relevant to the TA5+ years medical affairs, including medical education experience at regional levelExperience in alliance environments is a plus.Local Operating Company experience is requiredJOB LOCATIONThe role is EMEA based and is likely to involve extensive EMEA and International travel.The role holder will be expected to be based in his/her current country of residence as long as easy access to travel/transportation and local hosting is available at a J&J Commercial IM office.Required SkillsPreferred Skills:Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Product Strategies, Quality Assurance (QA), Research Proposals, Stakeholder Management, Strategic Thinking, Team Management #J-18808-Ljbffr