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Job Function:
Medical Affairs GroupJob Sub Function:
Medical Science LiaisonJob Category:
Scientific/TechnologyAll Job Posting Locations:
Madrid, SpainJob Description:
Johnson & Johnson, compañía líder en el sector, busca incorporar un profesional de Medical Scientific Liaison para su unidad de CART y Biespecíficos Mieloma Múltiple con residencia en Granada o Málaga.
Con el porfolio y pipeline más interesante del sector, J&J ofrece la oportunidad de formar parte de un proyecto innovador, puntero y referente dentro de la industria farmacéutica.
Como parte de Johnson & Johnson, nuestra misión es transformar la vida de los pacientes mediante el descubrimiento y desarrollo de soluciones innovadoras para cubrir las necesidades médicas más importantes de nuestro tiempo.
Buscamos incorporar profesionales con talento, ganas ilimitadas de contribuir, aprender, y buenos ¨team-players¨, dispuestos a afrontar cualquier reto y a lograr resultados excelentes. Buscamos personas que sean capaces de encontrar oportunidades y proactivamente fomentar su propio desarrollo.
Principales funciones que desempeñar:
To keep abreast of medical and scientific knowledge.
Continuous update on products, patient’s treatment trends, clinical activities and studies conducted within the therapeutic area in their region.
Development and maintenance of a contact network with Leading Specialists.
Understand their needs, key value drivers, practical treatment patterns and scientific activities within therapeutic area
Communicate value of company products, incl. clinical questionnaire discussions
Through scientific interactions, communicate medical benefits of products and contribute to foster innovative approaches
Represent the company within professional associations in the therapeutic area in cooperation with Medical Affairs/ Medical Education and other positions in the Medical Affairs Department
Proactive and reactive communication of medical scientific data according to following criteria
Proactive Scientific Communication to Leading Specialists must be consistent with the last approved Summary of Product Characteristics regarding the safe and effective use of approved products in approved indications. Content of Scientific Communication should be highly scientific, accurate, fair and objective, based on an up-to-date evaluation of all relevant evidence and reflect that evidence clearly, using neither marketing claims nor brand name.
In some very specific circumstances, the MSL can interact proactively with non-Leading Specialists. The program should be clearly defined in the MSL Country Activity Plan, providing the rational, the objective, content, timelines and selection criteria of the HCPs to be involved.
Description of R&D programs and discussing regulatory developments with no promotional intent are also part of Scientific Communication.
Reactive Communication of medical scientific data can be provided upon request to any Health Care Professional, within the approved label or off-label. The request should come either directly from the HCP or via the Medical Information department. MSLs are required to document all off-label information requests they receive from Leading Specialists and other HCPs that they may interact with.
Organization and participation in Medical Education activities, at local &/regional level:
Identify/support/educate speakers
Build Medical Education programs with scientific third party
Collaborate with Medical Education manager in National Medical education activities
Provide scientific material under request. MSLs may initiate discussion with potential speakers, discussing documents/ slides which may be of help for future presentations.
Organization and participation in Advisory Boards in cooperation with Medical Affairs/Medical Education/other positions in the Medical Affairs Department.
Market Access Discussions
MSLs can present highly scientific, accurate, fair and objective data to Payors (Hospital Formulary Committees, Health Insurers, Health Technology Assessment Committees, etc) to provide them with objective information about Company products.
Pre- Approval Activities
MSLs can engage in interactions with Payors to raise awareness so that payors can plan and budget so that patients can receive the product when it becomes available. MSLs can organize Speakers training to prepare speakers for delivering presentations to other HCP when the Marketing Authorization is granted.
Provision of scientific support to company Sales Representatives and other company representatives
Provide medical and product training and scientific support to Sales Representatives in coordination with Training/Medical Affairs Department as appropriate
Act as a reference point to Sales Representatives for any scientific query, in collaboration with Medical Information as appropriate.
Local implementation of Medical Affairs Plan in their areas:
Support the set up and follow up of local company sponsored studies, registries and other non-interventional Medical Affairs studies
Propose investigators and sites for interventional and non-interventional Medical Affairs studies.
Participate in investigator meetings preparation, recruitment follow-up and study result presentation.
Receive investigator proposals for IIS and ensure they are discussed within the Medical Affairs department for decision.
Through scientific interactions, gain valuable insight into treatment patterns and scientific activities in the therapeutic area and provide input and a strategic view to the company Medical Affairs Plan / business decision-making.
Observes and promotes all regulatory requirements as defined in applicable regulations, rules and procedures established by the Company, including but not limited to Health Care Business Integrity and Pharmacovigilance
Follow principles, procedures and training included in SAFE Fleet program.
GCO collaboration: Support GCO studies when needed through the identification of potential sites and facilitating a direct contact with leading specialists.
Report all suspected adverse reactions, serious or non serious, I may be aware of within a maximum of 24 hours after being aware of it and communicate it to the Pharmacovigilance Department.
Additionally, for all employees involved in Research Related Activities (RRA):
Ensure safety reporting requirements (timely AE/PQC reporting) as set out in company policies and SOPs (Standard Operating Procedures) are met and appropriately managed when planning projects, developing materials, executing projects and contracting vendors.
Ensure HCC and legal requirements (Fair Market Value, Transfer of Value rules, Promotional Materials rules) are fully understood, appropriately managed and complied with when planning projects, developing materials, executing projects and contracting vendors.
Ensure inspection readiness with respect to personal training compliance, and availability of recent CV and individualized Job Description.
Qualifications
Scientific degree: Medical Doctor, Pharmaceutical or Nature Science university degree, or related qualification (i.e. psychology degree)
Deep knowledge of the therapeutic area, strength in research and interpretation of medical data
Background to be accepted by the Leading Specialists in peer-to-peer relationship, i.e. relevant work experience, scientific acumen and/or communication skills.
Highly customer focused with an awareness of the importance of business results
Innovative with the ability to coordinate and drive a complex and changing environment
Awareness of, and adherence to, Johnson & Johnson Credo values and International Health Care Business Integrity Guide.
Special Requirements
Deep scientific knowledge in the therapeutic area
Required Skills:
Preferred Skills:
Analytical Reasoning, Analytics Insights, Clinical Data Management, Clinical Trials, Collaborating, Communication, Data Reporting, Detail-Oriented, Digital Culture, Digital Literacy, Execution Focus, Market Research, Medical Affairs, Medical Communications, Medical Compliance, Product Knowledge, Relationship Building, Scientific Research, Technologically Savvy