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MAIN RESPONSIBILITIES:
Leads efforts to define and implement medical strategies for the Infectious Disease in EMEA.
Creates and executes annual plan.
Identifies and establishes relationships with opinion leaders involved disease states or technical initiatives across the region.
Writes study protocols; monitors study progress; analyses results and works with investigators to publish papers. Works and publications must be accepted as medically important and useful in moving accepted science forward and/or influencing medical policy.
Must be recognized as a subject matter expert in field and as such collaborate with other key opinion leaders.
Prepares medical posters and abstracts and presents at key professional meetings in the Region.
Leads cross functional team involved in developing patient and physician education materials.
Acts as a liaison between Customers/Quality/Regulatory and technical organizations when medical issues arise.
Leads efforts of the Medical Affairs Managers located in EMEA Region.
Must comply with and enforce all Office of Ethics and Compliance guidelines.
As a senior member of the Medical Affairs organization, this role establishes contacts with key scientists around EMEA.
Provides input to the design of new products; technologies and OEM opportunities.
Identifies and recommends opportunity to gain additional product claims to improve medical utility.
EDUCATION:
Doctorate Degree ( 19 years)
Medical Doctor
EXPERIENCE:
5-10 years product development/medical management experience.
2-4 years business unit or general management experience.
Knowledge of regulations and standards affecting IVDs and Biologics.
Must have previously developed external relationships with key scientists or medical professionals.
Must have previously established and executed on Medical Affairs and/or R&D plan.
Industry, product, and customer knowledge required.
Must have strong interpersonal skills, good communication skills and medical writing skills.
Demonstrated leadership capabilities.
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