Medical Advisor Position
7 days ago
Company Overview:
Allergan is a leading company in the pharmaceutical industry, dedicated to discovering and delivering innovative medicines and solutions that solve serious health issues.
Job Description
- Provide specialist medical/scientific strategic and operational input for Hong Kong, into core medical affairs activities such as healthcare professional/provider interactions, educational initiatives, and safeguarding patient safety.
- Develop and maintain in-depth knowledge of assigned products/therapeutic areas through attendance/participation at key internal meetings/training sessions, relevant congresses, and seminars, and regular self-study of the literature.
- Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information, contributing to the review and medical and scientific accuracy of core dossiers, and supporting internal teams to develop their scientific and technical expertise.
- Establish and maintain professional and credible relationships with key thought leaders/external experts and academic centers, participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion fora, and delivering scientific presentations and medical education programs to healthcare professionals individually or in groups.
- Screen relevant literature and other information from scientific societies meetings and conferences, developing summaries of key messages for use within the brand team, and deliver training to sales forces and other departments, developing and updating relevant training materials.
- Involved in the Medical/Brand planning process for assigned Brands and therapeutic areas, ensuring all planned projects/scientific activities are carried out, with budgets, timelines, and compliance requirements factored into completion.
- Clinical Research Activities: Design and implement clinical research projects within defined standards and budgets, providing oversight to manage review, approval, and conduct of IIS studies, supporting the affiliate Clinical Research Department in the management of clinical studies, reviewing new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys, and monitoring the environment for competitive intelligence.
- Review promotional and preparation of non-promotional material, ensuring medical/scientific content is correct and fully compliant with Abbvie's internal policies and guidelines, providing medical/scientific input into marketing strategy and key commercial initiatives, as required, and ensuring compliance with all applicable laws and regulations, guidelines, codes of conduct, AbbVie's policies and procedures, and accepted standards of best practice.
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