Sr. Medical Affairs Scientist
1 semana atrás
Sr. Medical Affairs Scientist (MAS) Vaccines & IM - 6-month Secondment / Temporary ContractThe key responsibilities in this role include: Is responsible for the medical plans of the products assigned and its execution.Is responsible for all medical projects of the products assigned (including advisory boards, educational programs, etc.) and the respective direct budget monitoring.Performs the Global Medical Grants (GMG) medical reviews and is the owner of medical studies and other data generation projects for the products assigned, including real world evidence.Leads medical to medical communications and is the medical expert for Health Care Professionals (HCPs) and Medical Societies – is the key point of contact for external proactive and reactive medical interactions (face-to-face – F2F and digital) with selected HCPs. Has relevant medical-to-medical (M2M) discussions about the therapeutic area (including diagnostic and therapeutic guidelines), medical challenges and data gaps, patient education needs, healthcare environment and future trends in the respective medical field. Is responsible for organizing and conducting clinical sessions, as project owner, speaker, or moderator. Supports the commercial speakers' program initiatives by conducting speakers' briefings.Is the responsible for the development and continuous update of a stakeholder's plan (compliant with GDPR and Pfizer requisites) according to the medical specialties in scope.Timely creates up to date M2M content and tailored HCPs and patients' materials/solutions for F2F and digital interactions, approved through the adequate review & approval system. Is responsible for the scientific content creation to be used in the omnichannel strategy defined for the products assigned.Provides timely update of the medical interaction tool, following up on the HCPs' questions/insights/topics of interest and ensuring a constant flow of M2M relevant discussions.Collaborates closely with all medical areas to ensure sharing of medical knowledge and cross-pollination of best practices and innovative ideas.Aligns, supports, and contributes to different internal stakeholders:
collaborates and participates in working groups or other activities led by the Global and Chief Medical Affairs Office (CMAO) International Development Markets (IDM) Medical Teams for the assigned products.is the products' assigned medical point of contact for the cross-functional teams in the therapeutic area.provides medical input and medical strategic view to the Commercial area for the products assigned.works with Access&Value (A&V) in studies and reimbursement dossiers.collaborates with Regulatory in all the activities in the products' lifecycle that require medical related input, review and/or approval.collaborates with Supply Chain Quality (SCQ) in all the activities in the products' lifecycle that require medical related input, review and/or approval.collaborates with Medical Information and Drug Safety Unit in special requests for which local medical affairs input or review is required.is responsible for the internal medical training of all the assigned products.performs any other activity that requires medical input, review or approval for which is nominated by the Medical Team Lead.Is a key contributor to ensure company's medical compliance in internal projects and external engagements.Works closely with the Medical Quality Governance Manager (MQGM), Compliance, Legal and all cross-functional teams.REQUIRED SKILL SETUniversity Degree in health or life science areas.Minimum of 2 years of experience in the Pharmaceutical Industry or in relevant healthcare sector activities.Proven experience in the following areas:Medical plans and budget management.Medical governance and cross-functional teams' collaboration.Medical writing and comprehensive medical review of documents.Communication skills to different stakeholders and across different channels.External engagement competencies, including networking and stakeholders mapping & management.Performance driven with professional demeanor and strong collaboration skills.Ability to focus on priorities, resilience, organization, and project management competencies.Sense of responsibility and accountability, quality orientation.Strategic, agile, innovative and growth mindset.Language Requirements: Fluent in Portuguese and English.#LI-PFE Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here
#J-18808-Ljbffr
-
Senior Medical Affairs Scientist
Há 1 mês
Lisboa, Portugal Pfizer Tempo inteiroSenior Medical Affairs Scientist (Sr. MAS) – Breast Cancer (Temporary Contract/Secondment) 9 months The key responsibilities in this role include:Responsible for the medical plans of the products assigned and its execution.Responsible for all medical projects of the products assigned (including advisory boards, educational programs, etc.) and the...
-
I&i - Senior Medical Affairs Scientist (Sr. Mas)
3 meses atrás
Lisboa, Portugal Pfizer Tempo inteiro**Job Description**: - MAIN REPONSIBILITIES / DUTIES- The key responsibilities in this role include: - Is responsible for the medical plans and execution of medical scientific strategic plans of the products assigned - Is responsible for the scientific content creation to be used in the omnichannel strategy defined for the products assigned - Is responsible...
-
Medical Affairs Operations Specialist
3 meses atrás
Lisboa, Portugal Pfizer Tempo inteiroThe Medical Affairs Operations Specialist will partner with the relevant Medical Affairs Departments within the Western European Cluster (WEC) as needed, to provide comprehensive organizational, project management and administrative expertise to ensure compliant and efficient operation and execution of Medical Affairs activities carried out in these...
-
Lisboa, Lisboa, Portugal Pfizer Tempo inteiroJob Summary Pfizer is seeking a highly skilled Medical Affairs Operations Specialist to join our team in Western Europe. The successful candidate will be responsible for providing comprehensive organizational, project management, and administrative expertise to ensure compliant and efficient operation and execution of Medical Affairs activities in the...
-
Medical Affairs Operations Specialist
4 semanas atrás
Lisboa, Portugal Buscojobs Portugal Tempo inteiroPOSITION SUMMARYThe Medical Affairs Operations Specialist will partner with the relevant Medical Affairs Departments within the Western European Cluster (WEC) as needed, to provide comprehensive organizational, project management and administrative expertise to ensure compliant and efficient operation and execution of Medical Affairs activities carried out...
-
Vaccines & Antivirals - Sr Medical Affairs
3 meses atrás
Lisboa, Portugal Pfizer Tempo inteiroMAIN REPONSIBILITIES / DUTIES The key responsibilities in this role include: - Is responsible for the medical plans and execution of medical scientific strategic plans of the products assigned - Is responsible for the scientific content creation to be used in the omnichannel strategy defined for the products assigned - Is responsible for all medical...
-
Medical Affairs Trainee Specialist
Há 7 dias
Lisboa, Lisboa, Portugal Biogen Tempo inteiroMedical Affairs Trainee RoleThe Medical Affairs Trainee is an integral part of the Medical Department, offering the opportunity to work within the Neurology and Rare Diseases Therapeutic Areas, with a particular focus on Multiple Sclerosis and Spinal Muscular Atrophy.This internship provides a valuable platform for developing communication skills with both...
-
Medical Affairs Operations Specialist
3 meses atrás
Lisboa, Portugal Pfizer Tempo inteiroPOSITION SUMMARY The Medical Affairs Operations Specialist will partner with the relevant Medical Affairs Departments within the Western European Cluster (WEC) as needed, to provide comprehensive organizational, project management and administrative expertise to ensure compliant and efficient operation and execution of Medical Affairs activities carried out...
-
Medical Affairs Advisor
4 meses atrás
Lisboa, Portugal Somaí Pharmaceuticals Ltd. Tempo inteiroSOMAÍ Pharmaceuticals is an EU-GMP Portuguese manufacturer of cannabinoid formulations for the international markets. At SOMAÍ, the world is changing fast toward regulating and legalizing medical cannabis – and we want to be one step ahead of the curve. That's why we're deeply committed to providing the best medical cannabis products of tomorrow to our...
-
Medical Affairs Trainee
2 semanas atrás
Lisboa, Portugal Biogen Tempo inteiroJob Description About This Role The Medical Affairs Trainee role is an integral part of the Medical Department, offering the opportunity to work within the Neurology and Rare Diseases Therapeutic Areas, with a particular focus on Multiple Sclerosis and Spinal Muscular Atrophy.The trainee will actively participate in implementing the medical strategy and...
-
Medical Affairs Trainee
3 meses atrás
Lisboa, Portugal Novo Nordisk Tempo inteiroMedical Affairs trainee **Category**:Education**Location**:Lisbon, Lisbon, PT**The position** - You will be able to actively support the implementation of Novo Nordisk Healthier Portugal strategy. As a Medical Affairs Trainee at Novo Nordisk, you will: - Provide timely and high-quality Medical Information to Key Opinion Leaders (KOLs) and other HCPs. -...
-
Global Medical Affairs Director
Há 1 mês
Lisboa, Lisboa, Portugal Organon Tempo inteiroJob OverviewWe are seeking a highly skilled Global Medical Affairs Director to join our team at Organon.
-
Medical Affairs Advisor
4 meses atrás
Lisboa, Portugal Somaí Pharmaceuticals Ltd. Tempo inteiroSOMAÍ Pharmaceuticals is an EU-GMP Portuguese manufacturer of cannabinoid formulations for the international markets. At SOMAÍ, the world is changing fast toward regulating and legalizing medical cannabis – and we want to be one step ahead of the curve. That's why we're deeply committed to providing the best medical cannabis products of tomorrow to our...
-
Medical Scientist Specialist
Há 1 mês
Lisboa, Lisboa, Portugal Gilead Sciences Tempo inteiroAbout the RoleWe're seeking a Medical Scientist to join our team at Gilead Sciences, a leading biopharmaceutical company. In this role, you will be responsible for managing clinical inquiries regarding marketed or developmental products, presenting scientific and clinical data, and establishing strong relationships with opinion leaders and clinical...
-
Medical Affairs Manager
7 meses atrás
Lisboa, Portugal Johnson & Johnson Tempo inteiro**For our pharmaceutical sector, we are currently recruiting a Medical Affairs Manager (M/F) - Immunology on a permanent contract. The role is based in our Lisbon office.** **OVERALL PURPOSE OF THE JOB**: To plan, coordinate, and execute Medical Affairs Plan, including research and publication programs conducted by Medical Affairs. To be a therapeutic area...
-
Trainee - Medical Affairs Officer
6 meses atrás
Lisboa, Portugal Viatris Tempo inteiroMylan, Lda. At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access - Providing high quality trusted medicines regardless of geography...
-
Medical Affairs Trainee
Há 1 mês
Lisboa, Lisboa, Portugal Novo Nordisk AS Tempo inteiroAbout the RoleWe are seeking a highly motivated Medical Affairs Trainee to join our team in Lisbon. The ideal candidate will be a recent graduate or finishing a bachelor's degree/master/PhD program, in Pharmacy or a related field in Life Sciences.Key ResponsibilitiesProvide timely and high-quality Medical Information to Key Opinion Leaders (KOLs) and other...
-
Sr. Scientist, Regulatory Affairs
3 semanas atrás
Lisboa, Portugal Biom?Rieux Bv Tempo inteiroSr. Scientist, Regulatory Affairs - Chemistry, Manufacturing & Controls (CMC) The Senior Scientist is responsible for implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned products in accordance with global regulations, guidance's, and defined regulatory strategies. The Senior Scientist is responsible for the preparation...
-
Sr. Scientist, Regulatory Affairs
3 semanas atrás
Lisboa, Portugal Biom?Rieux Bv Tempo inteiroSr. Scientist, Regulatory Affairs - Chemistry, Manufacturing & Controls (CMC)The Senior Scientist is responsible for implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned products in accordance with global regulations, guidance's, and defined regulatory strategies. The Senior Scientist is responsible for the preparation...
-
Lisboa, Lisboa, Portugal Novo Nordisk Tempo inteiroOverviewNovo Nordisk is a leading pharmaceutical company that doesn't wait for change, it drives it. As a Medical Affairs Director with Regulatory Expertise, you will play a pivotal role in shaping the future of patient care.
