Medical Affairs Specialist
Предложен/а от:
На разположение за събитието:
Описание на предложението за работа
- Advance science and standards of care for patients, healthcare providers and - if approbate - payers
- Enhance the scientific credibility of the company with established and emerging national and regional thought leaders
- Provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts of strategic importance to AbbVie
- Act as the point of contact with thought leaders to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate
- Develop and maintain collaborative relationships with thought leaders in the product / therapeutic area for which the MSL has been assigned responsibility, to facilitate AbbVie research and educational priorities
- Interact with marketing and sales of assigned product and therapeutic area; Market access teams; Brand teams, Government Affairs; Public Affairs; Regulatory Affairs; Legal; OEC.
- Support internal teams such as sales and marketing and members of the Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations
- Work collaboratively and cross-functionally with other in-field members while retaining functional independence
- Interface with other key members of the affiliate medical department - for example: Medical Managers, Medical Advisors, Clinical Research Managers, Library Information Specialists and others as appropriate - relevant to the therapeutic area for which the MSL has responsibility
Условия на работата
- Advanced degree (e.g. PharmD., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered
- Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company
- Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research
- Experience working in pharmaceutical industry (advantage)
- Experience in out-of-office functions desirable
- Basic knowledge of project management
- Good understanding in written and oral English
- Perfect knowledge of the local language
- Computer and software knowledge like MS Office (Word, Excel, PowerPoint, Outlook) as well as Lotus notes and other software, Internet