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Job Description

PRIMARY FUNCTION: Represent the affiliate’s medical/scientific voice of expertise for assigned product(s) and relevant therapeutic areas. Provide medical/scientific expert advice/guidance to key customers for assigned products and relevant therapeutic areas, including scientific exchange and professional relationship development with key thought leaders and external experts. Provide medical/scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical/scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross‑functional affiliate teams. If relevant, provide leadership, strategic direction and mentorship to direct reports, as appropriate, and fulfill line management responsibilities accordingly. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.

Responsibilities

- Develop and maintain in‑depth knowledge for assigned product(s) and relevant therapeutic area(s) through attendance and participation at key internal meetings, training sessions, relevant congresses, seminars, and by regular self‑study of the national and international literature.
- Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific or technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews, etc.).
- Establish and maintain professional and credible relationships with key thought leaders, external experts and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round‑table meetings,



discussion fora, etc.
- Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.
- Screen relevant literature and other information from relevant scientific societies, meetings and conferences and develop summaries of key messages for use within the Company (key areas of scientific or company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.).
- Deliver training to sales forces and other departments; develop and update relevant training materials.
- Review and preparation of promotional material. Ensure the medical/scientific content is correct and fully compliant with AbbVie’s internal policies and guidelines.
- Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.
- Monitor the environment for competitive intelligence (product strategies, studies, commercial messages, positioning, etc.) and communicate, where appropriate, within the Company.
- Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures and accepted standards of best practice.
- Provide input, as required,



into the development of product or therapeutic‑area specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products and therapeutic areas are aligned with local business‑related strategic plans.
- Ensure that local medical affairs implementation plans for assigned products and therapeutic areas are executed efficiently.
- Provide leadership, line management and development for direct reports, as appropriate.
- Operate as a scientific interface and resource to HCPs, health care institutions, external experts and professional associations regarding assigned AbbVie products or products in development.
- Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific information.

Clinical Research Activities

- Design and implement clinical research projects within defined standards and budgets (e.g., PhaseIV, post‑marketing clinical activities such as registry/database projects, epidemiological surveys and PMOS studies).
- Provide oversight to manage review, approval and conduct of IIS studies.
- Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (review new clinical study protocols, identify potential investigators/sites, conduct feasibility surveys).

Accountability & Scope

- Provide input, as required, into the development of product or therapeutic‑area specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate with local business partners to ensure alignment.
- Ensure that local medical affairs implementation plans for assigned products and therapeutic areas are executed efficiently.
- Provide leadership, line management and development for direct reports, as appropriate.
- Ensure adherence to all applicable national laws and regulations, guidelines and codes of conduct as well as AbbVie standards, policies and procedures.

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Postúlate en Kit Empleo: kitempleo.cl/empleo/1dooti

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