MSL/Disease Area Advisor Oncology (Fixed-Term contract)

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAre you looking for a patient-focused, innovation-driven company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a MSL/Disease Area Advisor Oncology (Fixed-Term contract).Takeda is a global pharmaceutical leader with more than 50,000 professionals working together across more than 80 countries. We have an unwavering dedication to put people first and we live our values of Takeda-ism: Integrity, Fairness, Honesty, and Perseverance. We are united by our more than 240-year legacy of research-based pharmaceuticals and our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine in rare diseases.ABOUT THE ROLE:The Medical Science Liaison is responsible for managing projects and processes related to medical products throughout their lifecycle. By ensuring effective product performance and adjustments, this role supports Takeda's mission to bring better health to people.Med. Advisor:Provide medical expertise and support for Therapeutic Area/ Takeda products of responsibility to Market Access, Marketing & KAMs and other internal stakeholders.Support the Portuguese Disease Area Lead Oncology in establishing the local Medical Strategy Plan and its implementation for the TA of responsibility.Ensure the correct interpretation and communication of scientific data of Takeda products.Advocacy for patients needs.Provide TA leadership.Medical Scientific Liaison:Provide local country field-based support from the medical function in order to achieve the company's goals.Identify and develop strong sustainable peer-to-peer relationships with external stakeholders to support the medical/scientific credibility of the company.ACCOUNTABILITIES:Continuously screen, review and analyze scientific literature; generate summaries & critical assessments if appropriate.Use specific disease and product knowledge to develop Takeda in a given therapy area.Proactively identify and develop long-term peer-to-peer relationships with opinion leaders and other relevant stakeholders (KOLs, HSEs, HCPs, patient organizations).Act as field-based reference points of scientific and clinical expertise for sales force and other internal stakeholders.Support ongoing and future Company Sponsored Studies.Capture and share in-field insights to support medical and scientific strategy and business development.Participate in the development and implementation of key medical activities.Provide clinical presentations and medical information as necessary.Facilitate unsolicited requests from HCPs for investigator-initiated sponsored research proposals.Development and support of national disease registries and RWE projects for relevant disease areas.Understand leverage points of the patient journey.Medical/Scientific Affairs:Present the clinical evidence to internal and external stakeholders in a non-promotional way.Assess scientific accuracy and validity of non-promotion material.Develop local strategic medical plans in line with product Life Cycle Management plans.Act as communication link to authors of scientific publications about Takeda products.Provide extensive, clear and structured briefing to external presenters/speakers at Takeda sponsored medical events.Identify gaps in the local clinical study program.Provide medical expertise to LOC Market Access.Provide medical expertise to LOC Regulatory Affairs/LOC Pharmacovigilance/LOC Quality Assurance.Evaluate and support local investigator initiated research proposals.Budget responsibility for medical affairs activities related to TA/product.Other medical and scientific support duties as assigned.Provide scientific input into Marketing strategy and tactics.Provide medical input for development of promotion material.Assess scientific accuracy and validity of promotion material.Cross-functional Collaboration:Ensure awareness and communication of medical activities to other departments within the Local organization.Participate in local product committees and brand planning cycles.Clinical Development:Develop study outline and protocol for local post-authorization and other RWE studies.Liaise with CROs and other vendors for Takeda sponsored global studies.Collaborate with Global Development Operations functions.Medical Information:Maintain a tracking system for all unsolicited medical enquiries.Provide timely, accurate and balanced answers to unsolicited medical enquiries.Collaborate with Regional and Global Medical Information.Act according to Corporate, Compliance, Ethical codes and Legal standards.Promote and demonstrate commitment to Takeda-ism philosophy and values.Communicate to pharmacovigilance department any adverse reaction.Ensure development and implementation of an annual quality plan.EDUCATION, EXPERIENCE, SKILLS, KNOWLEDGE:Education:University degree in Science or Pharmacy (mandatory).PhD or Master's Degree in a biological or medical science or medical qualification (Desirable).Experience:Experience in pharmaceutical industry (Desirable minimum 2 years).Experience of working in a matrix management environment.Experience with therapies in Oncology.MSL or equivalent medical affairs experience (Desirable).Clinical trials experience and good understanding of clinical trial data and study design (Desirable).Experience of working with scientific and clinical experts at all levels (Desirable).Experience in providing clinical data and disease area training (Desirable).Skills:Fluent written and spoken English (mandatory).Ability to work at a high scientific and clinical level.Clear and concise presentation of clinical data.Autonomous, in-field work.Project management skills.Rapid assimilation of information.Ability to influence at high level.Strong interpersonal skills.Drives performance of self and others.Highest ethical standards.IT skills (Microsoft Word, Excel and PowerPoint).Knowledge:Understanding of clinical trials process and research infrastructure in Oncology (Desirable).Thirst for technical, clinical, medical and scientific knowledge (Desirable).LocationsLisbon, PortugalWorker TypeEmployeeWorker Sub-TypeTemporary / Limited TermTime TypeFull time

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