Pharmaceutical Medical Affairs Expert

2 days ago

Petaling Jaya, Selangor, Malaysia Allergan Full time

About the Role:

The Pharmaceutical Medical Affairs Expert will be responsible for providing medical/scientific input into marketing strategy and key commercial initiatives, staying up-to-date on the latest developments in oncology, and communicating findings to colleagues and partners. This role requires strong analytical, problem-solving, and critical thinking skills, with the ability to evaluate complex data and draw meaningful conclusions.

Key Responsibilities:

  • Develop and maintain in-depth knowledge of assigned products/relevant therapeutic areas through attendance/participation at key internal meetings/training sessions, relevant congresses, and seminars, as well as regular self-study of national/Area literature.
  • Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information, and contributing to the development and medical/scientific accuracy of core dossiers generated by the medical department.
  • Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations, working collaboratively and cross-functionally with other in-field members while retaining functional independence.
  • Establish and maintain professional and credible relationships with key thought leaders/external experts and academic centers, involving participation in scientific congresses, coordination of 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.
  • Deliver training to sales forces and other departments, developing and updating relevant training materials.
  • Involved in the Medical/Brand planning process for the assigned Brand and therapeutic areas, ensuring that all planned projects/scientific activities are carried out, factoring in all budgets, timelines, and compliance requirements for project completion.
  • Clinical Research Activities:
    • Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, 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 managing clinical studies, as necessary (e.g., reviewing new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).
  • Review and preparation of promotional/non-promotional material, ensuring 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, monitoring the environment for competitive intelligence (e.g., product strategies, studies, commercial messages, positioning, etc.) and communicating appropriately 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.

Accountability & Scope:

  • Provide input into the development of product-specific strategic medical affairs plans for the affiliate medical department and local commercial plans, collaborating and partnering with local business partners to ensure medical activities for assigned products/therapeutic areas align with local business-related strategic plans.
  • Ensure local medical affairs implementation plans for assigned products/therapeutic areas are executed efficiently.
  • Lead, line-manage, and develop direct reports, as necessary.
  • Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.
  • Operate as a scientific interface and resource to HCPs/Customer(s), 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 data, educational initiatives, and patient safety for assigned products/therapeutic areas.

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