The Medical Advisor provides medical/scientific strategic and operational input within Israeli the affiliate into core medical affairs activities such as: healthcare professional/provider interactions; generation of clinical and scientific data; educational initiatives; safeguarding patient. Provides strategic medical input into core brand (product) strategies and to support market access and medical/marketing activities.
Responsibilities:
- Develop and maintain in-depth knowledge of the companys products and provide professional Medical Information to internal and external interfaces.
- Develop medical strategy planning and implementation of medical activities in accordance with business priorities of GMA and the BT.
- Organize and moderate advisory boards lectures and scientific/medical events/ education.
- Establish develop and maintain strong professional relationships with key external stakeholders including relevant key opinion leaders
- Deliver scientific presentations to KOLs and/or related medical units
- Participate in scientific conferences and meetings related to the therapeutic area.
- Prepare for the launch of new products including preparation of the relevant sections in the file submission to MOH
- Review and approve promotional material of products related to the expertise area and support the marketing department in the preparation of materials.
- Clinical Research Activities:
- Design and implement clinical research projects within defined standards and budgets
- Provide the required oversight to manage review approval and conduct of IIS studies.
- Support the affiliate Clinical Research Department in the management of clinical studies as appropriate
Qualifications :
- Medical Doctorate (M.D.) degree or equivalent with relevant therapeutic specialty Completion of residency and/or fellowship is preferred.
- Minimum of 2 years of medical affairs experience in the pharmaceutical industry
- Proven leadership skills in a cross-functional global team environment. Ability to interact externally and internally to support global business strategy. Ability to run a clinical study or medical affairs team independently with little supervision.
- Knowledge of clinical trial methodology regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
- Good presentation skills
- Excellent interpersonal skills
- Confidence Enthusiasm
- Ability to operate as a flexible team player
- Fast learning and implementation of new scientific material
- Ability to bring initiatives to advance medical company agenda
- Excellent oral and written English communication skills.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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Work :
No
Employment Type :
Full-time