Specialty Care & Internal Medicine Medical Lead, Misp Cluster

Pfizer Pfizer · Pharma · Kuala Lumpur, Malaysia

Pfizer is seeking a Specialty Care & Internal Medicine Medical Lead for the MISP cluster (Malaysia, Indonesia, Singapore, Philippines) to provide medical leadership, develop and execute strategy, and manage the medical team. The role involves cross-functional collaboration with commercial, regulatory, safety, and legal teams, providing medical guidance for product maintenance and defense, and developing strategic partnerships with stakeholders. The lead will also initiate and manage pilot projects for launch excellence and regional medical initiatives, oversee the therapy area medical budget and headcount, and ensure medical quality and compliance. Requires over 7 years of medical affairs experience in pharmaceuticals, with expertise in regulatory/safety risk management, understanding of local health environments and codes of practice, and knowledge of pharmacovigilance and regulatory legislation. An MD is required, with other advanced clinical degrees or an MBA being a plus. Fluency in English is necessary, and local language fluency is preferred. Strong analytical, organizational, communication, and leadership skills are essential, along with the ability to travel within the cluster.

What you'd actually do

  1. Provide medical leadership to the Specialty Care & Internal Medicine medical team & responsible for developing and executing the MISP Specialty Care & Internal Medicine Medical Team’s vision and strategy in alignment with the Commercial Lead.
  2. Manage high performing MISP Medical organization and will ensure that country medical functions systems, processes & activities are fully aligned with country business priorities, strategies and needs, as well as, in compliance with corporate policies, SOPs & guidelines.
  3. Serve as the key Country liaison with country/cluster/regional/HQ Commercial, Medical, GMPE, Clinical Affairs, Regulatory, Safety, Corporate Affairs and, Legal functions.
  4. Provide medical guidance and input to the regulatory, safety and commercial leadership teams in support of key product maintenance & defense activities.
  5. Develop strategic partnerships with key clinical and other stakeholders; developing strategies aligned to customer needs in order to maintain a therapeutic leadership position and drive business needs at the country level.

Skills

Required

  • Medical leadership
  • Strategy development and execution
  • Cross-functional collaboration
  • Product portfolio management
  • Medical quality and compliance
  • Stakeholder engagement
  • Regulatory affairs
  • Safety risk management
  • Pharmacovigilance
  • Pharmaceutical industry experience
  • English fluency
  • MD degree

Nice to have

  • Regional experience
  • Local language fluency
  • MBA
  • Advanced clinical degree

What the JD emphasized

  • medical affairs function in the pharmaceutical industry with broad expertise in medical & experience with regulatory and/or safety risk management issues
  • Understanding of the local health environment & knowledge of the relevant and applicable local and regional Codes of Practice, SOPs, regulations and guidelines within the cluster
  • Knowledge of pharmacovigilance & regulatory legislation and how it impacts product portfolio
  • MD is a requirement