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 :
- PHD DMD DVM Pharm.D or MD degree or equivalent with relevant therapeutic specialty.
- 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 Culture
At AbbVie we care deeply about bringing innovative solutions to patients in need. By joining us youll be at the forefront of our mission working in a dynamic and supportive environment that encourages growth and collaboration.
- All4OneAbbVie: Foster strong interpersonal relationships and teamwork.
- Decide Smart & Sure: Navigate ambiguity and make informed decisions.
- Agile & Accountable: Communicate a clear and inspiring vision.
- Clear & Courageous: Provide honest and constructive feedback.
- Make Possibilities Real: Efficiently plan and execute tasks while adapting to challenges.
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