Medical Advisor / MSL Oncology
Ipsen · Budapest
Titre : Medical Advisor / MSL Oncology Société: Ipsen Pharma Hungary Kft.
A propos d'Ipsen: Ipsen est un groupe biopharmaceutique mondial de taille moyenne, spécialisé dans les médicaments transformateurs dans trois aires thérapeutiques : l'oncologie, les maladies rares et les neurosciences. Forts de près de 100 ans d'expérience en développement, avec des Hubs mondiaux aux États-Unis, en France et au Royaume-Uni, nous focalisons nos efforts là où les besoins médicaux non satisfaits sont importants, grâce à la recherche et à l'innovation.
Nos équipes passionnées, présentes dans plus de 40 pays, se concentrent sur l'essentiel et s'efforcent chaque jour d'apporter des médicaments aux patients dans 88 pays. Nous construisons un environnement de travail qui met en avant un leadership centré sur l'humain et favorise une culture de collaboration, d'excellence et d'impact. Au sein d’Ipsen, chaque individu est encouragé à être soi-même, à grandir et à s’épanouir aux côtés du succès de l'entreprise.
Rejoignez-nous dans notre démarche vers une croissance durable, en créant un impact réel sur les patients et la société. Pour plus d'informations, visitez notre site web à l'adresse https://www.ipsen.com et suivez nos dernières actualités sur LinkedIn et Instagram. Description de l'emploi :
Summary & Purpose of the Position External and internal stakeholders delivering non-promotional information exchange, supporting data and insight generation to provide patient-centric solutions in assigned area. The MA/MSL is a scientific point of contact for the assigned therapeutic area internally in Ipsen, with focus on review of promotional and nonpromotional materials, medical training of internal stakeholders and other activities related to medical advisory role.
The MA/MSL must maintain up-to-date knowledge of relevant scientific information. The MA/MSL works in coordination with the rest of the Medical Department to meet the Medical Department objectives. Directs all aspects of organization´s medical policies, standards and programs and ensures all medical activities are compliant with all applicable local regulations.
Main Responsibilities
& Technical Competencies Support to clinical development & ISS (data generation) Coordinate and facilitate unsolicited Investigator‐Sponsored Study (ISS) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs’ objectives Support the R&D projects and Company Sponsored Studies (CSS) operations (investigators site identification and evaluation, feasibility studies, recruitment, investigator meetings, external expert identification, study management, investigators query) when appropriate Support the implementation and follow‐up of post-marketing clinical activities such as registry/database projects, epidemiological surveys, post‐authorization studies (phase IV) at the site level Identify opportunities to generate real‐world‐evidence data Ensure internal cross‐functional collaborations as a scientific partner Ensure development and maintenance of a medical and scientific information service in the key areas to provide support to Health Care Professionals Participate at brand teams´ work and campaigns preparation Provide inputs to the Medical Budget and Local Annual Medical plans, to participate on preparation of brand strategic plans with focus on their medical parts Keep high scientific profile and medical knowledge within assigned therapeutic area With the commercial staff (Marketing or Sales) to:
Provide scientific expertise and training to commercial staff as required Review promotional materials in accordance with the local SOP Contribute to the review and approval of non‐promotional materials in accordance with the local SOP Attend the local brand teams to bring additional scientific perspective Attend and contribute to regional account planning/training sessions Ensure speakers briefing for promotional meetings With Market Access department to:
Respond to requests to support hospital formulary submissions and upon request to present the data on Ipsen products Respond to scientific inquiries to deliver scientific presentations on the disease area and on the product Regulatory, Pharmacovigilance, Medical information In RA, cooperate with local service providers on revisions of prepared RA texts, local submissions. To provide Local Quality with consultancy support whenever requested.
In PV, cooperate with PV, RA and marketing on implementation of RMPs and aRMMs. To provide Local Quality with consultancy support whenever requested. Complete all pharmacovigilance trainings, ensure the accurate, timely reporting and follow-up activities of all adverse events and special situations reports.
To provide medical information support according to relevant IPSEN requirements, to use the MI system properly. To ensure high quality in providing MI services across therapeutic areas within the affiliate. Establish and foster professional collaborations with the Healthcare community Map the scientific expertise: identify, complete and update Thought Leaders (TL) database in assigned therapy area in accordance with the Global MSL Directive and the TL Tiering Process Conduct fair and balanced scientific exchanges with TL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings (congresses, symposia, etc.), potential research collaborations Identify opportunities for collaboration with TL when aligned with Ipsen strategy Develop and enhance scientific and educational collaborations with Healthcare Professionals (HCP) within the Healthcare community and act as a medical contact for TL and external medical experts Reactively respond to unsolicited and documented queries from HCP.
Record the medical inquiries in Medical Information System (MISTRAL) according to relevant SOP. Develop and/or implement unbiased and non‐promotional scientific exchange meetings and educational activities Provide sc