PT-Medical Expert Hematology Date: 18 Jul 2024
Medical Expert Hematology (m/f/x)
The Position
In your function you will act as the primary point of contact and the local key scientific expert for Quizartinib and AML disease with internal and external stakeholders in 'Country XYZ', in the Daiichi-Sankyo European Medical Affairs team and report directly to the Director European Medical Affairs Hematology (dotted line with the country relevant member).
This is a mixed position mainly based on MSL activities (70-80% on the field) and with national office-based activities (for example: national advisory board, a symposia, compliance for material approvals, HCP contracts, etc).
Key Responsibilities:
Communicate the Scientific value of hematological products (focus on Quizartinib), to internal and external stakeholders and have a customer-centric approach involving KEEs, nurses, scientific country AML collaborative groups
Mapping the Key External Experts (KEE) tier 1 and 2 as well as to establish and maintain professional relationships with medical and scientific opinion leaders and relevant medical societies
Support medical affairs activities and generation and dissemination of data to the main/key stakeholders
Discuss ISS with KEEs if there is a need aligned with the regional medical director
Ability to manage a country budget aligned with the regional medical director in line with company policies
To be the first point of contact in the country with hematologists
To be the expert regarding AML disease, treatments landscape, and Quizartinib medical value
Through scientific interactions, champion the medical value of hematology compounds (focus on Quizartinib) in the pipeline and contribute to the fostering of innovative approaches
Develop and execute an external stakeholder engagement plan aligned with the regional medical director in charge of Quizartinib
Coordinate and align successfully the cross-functional prelaunch and launch activities for Hematology compounds (focus on Quizartinib), including Market Access activities, such as support on value dossier, access at the regional level, and regulatory support
Set up local advisory boards and symposia around local key congresses aligned with the European strategy
Respond to scientific queries from Hematologists with regards to our hematological pipeline products in development, based on Medical Affairs and Medical Information documents
Support and manage Medical Affairs clinical activities strategy, planning, design, and execution (in close co-operation with HQ and CROs)
Contribute to the pre-launch and launch steps of new hematology products (providing scientific support)
Contribute and execute the R&D clinical trials (site selection, SIV, and follow up of clinical trials)
Could be involved to support the reimbursement dossier for a medical perspective if needed
Ensure compliance requirements are factored into programs' scientific activities
Express attitude to work in a cross-functional team
Conducts all activities in accordance with the applicable laws, rules, and regulations
Qualifications:
Scientific background (MD, PharmD, PhD, other scientific degree)
Experience as MSL or other roles in Medical Affairs/R&D is preferred
Oncology knowledge/expertise in hematology highly recommended
Experienced in communicating with medical-scientific opinion leaders
Ability to quickly and accurately learn, retain, and present detailed scientific information
Good skill in presenting, communicating, and facilitating discussions with small and large groups in an engaging manner
Field-based within the area of activity or available to definitively relocate
Ability to work in a matrix and multicultural organization
High self-motivation, assertiveness, and goal orientation
'Hands-on' mentality
Local Language plus Very Good English
Good understanding of local laws and procedures
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