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Senior Manager Medical Affairs Adjuvants (31567)
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Senior Manager Medical Affairs Adjuvants (31567) : MedImmune
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| Job Number |
57275 |
| Employee Type |
Full Time |
| Company Name |
MedImmune |
| Location |
Wavre
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
1/7/2010 |
| Industry |
Pharmaceutical |
| Job Type |
Other |
| Relocation |
Not Required |
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MedImmune
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| Description |
Basic Qualification • 5 to 10 years of experience in the pharma, preferably vaccine industry (being in clinical development, medical affairs, regulatory, project management, R&D…). • Medical Doctor or Post graduate scientific diploma (PhD) • Specialization in the fields of /or experience with vaccines, vaccine technologies, infectious diseases, immunology, preventive medicine and public health is a major asset • A team player or used to work in a matrix organisation • Fluent in English • Willing to learn Ability to deal with different topics at the same time and to promptly react to unexpected issues or business needs • Open-minded, flexible Attention to details while keeping the focus on portfolio view – Respect for rules and processes Details Job Purpose
Increases the recognition of the role of Medical Affairs in providing scientific vaccine expertise and adjuvants expertise to relay key messages for worldwide scientific and medical communities through publications, public presentations and interactions.
Responsibilities
• As medical business partner builds efficient interactions with other departments (Clinical, Epidemiology, Safety, R&D,…) - Manages the integration, standardization and harmonization of scientific key messages across different teams in a matricial structure - Ensure the processes ownership and consistency for internal processes such as: o Promotional material approval process (Promo Cap process) o Implementation of the essential messages, e.g. rationale, medical need, value of adjuvants in vaccine formulation within all publications, in particular to the ones generated by the medical affairs department - Participate in the development and implementation of the medical affairs communication plan - Ensure the operation alignment including scientific expertise, vaccinology,.. - Ensure the driving, the delivery and the maintenance of data and information publication through the internal communication platform (intranet) - Coordinate and guide the work of internal communication experts (in charge of the medical information), - Establish appropriate networks and contacts with key players from other departments (Clinical, EPI, Safety, R&D,…) and with External Experts (EEs) in order to be able to provide critical medical input that will contribute in improving vaccine positioning and competitiveness - Supervise the reviewing and give formal approval for medical answer communication pieces such as: answers to LOC questions, standard letters, monographs, position papers, publications, presentations, answers to questions for internal and external audiences - Drive the organization of Advisory Board meetings
• Acting as a medical affairs reference partner for GSK LOCs and GSK Regional offices: - Supporting regional and local organizations on general medical issues beyond the scope of competences of the local or regional offices. - Provide medical training and coaching on vaccination and adjuvants to selected medical partners in GSK regional and LOC offices - Organize and make available core medical materials and regularly updated product data packages for GSK LOCs/Regions - Provide medical support to crisis management (Urgency plans)
• Being an ambassador and influencer for vaccination in general and for GSK vaccines in particular, through network with Experts, Health Officials, Policy Makers and Clinicians: - Scientific presentations to international audiences - External Experts (KEE) contact and management - Attendance of key medical congresses These activities support the position of GSK Biologicals as a major vaccines developer and supplier and enhance the scientific and humanistic image of GSK Corporate.
• Responsibility for providing Medical Affairs support together with his/her team: - Coach the Internal and/or the External Communication Scientists on Standard Letters, position papers, publications, presentations and answers to questions for internal and external audiences. - Provide the criteria for the selection and updating of the GSK Bio literature database - Contribute to the overall establishment of global practices and operational excellence throughout the WW Medical Affairs Team - Facilitate team work and contribute to a positive attitude and team spirit
• Ensure adherence to medical compliance (codes, SOP’s) of all actions and events related to medical and scientific interactions where the Franchise or the WW Medical Affairs Department is involved |
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| Requirements |
Preferred Qualification • 5 to 10 years of experience in the pharma, preferably vaccine industry (being in clinical development, medical affairs, regulatory, project management, R&D…). • Medical Doctor or Post graduate scientific diploma (PhD) • Specialization in the fields of /or experience with vaccines, vaccine technologies, infectious diseases, immunology, preventive medicine and public health is a major asset • A team player or used to work in a matrix organisation • Fluent in English • Willing to learn Ability to deal with different topics at the same time and to promptly react to unexpected issues or business needs • Open-minded, flexible Attention to details while keeping the focus on portfolio view – Respect for rules and processes |
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