Drug Safety Unit Cluster Lead

7 days ago

Kuala Lumpur, Kuala Lumpur, Malaysia Pfizer, S.A. de C.V Full time
Job Title: Drug Safety Unit Cluster Lead

Pfizer, S.A. de C.V is seeking a highly skilled and experienced professional to lead our Drug Safety Unit Cluster. As a key member of our team, you will be responsible for managing and providing strategic direction to the pharmacovigilance teams within the cluster.

Key Responsibilities:
  • Lead and manage the Cluster along with the Country Safety Lead role.
  • Develop and enhance the capabilities and capacities of the team through the identification and implementation of training and development needs.
  • Manage and Co-ordinate work-sharing within cluster.
  • Strategic management of Cluster resources in collaboration with platform and WWS leadership.
  • Provides guidance to CSLs for projects/decisions impacting safety reporting at country level.
  • Engage and provide guidance to the CSL network.
  • Engages in cluster level network with functions beyond safety (e.g.: quality, CEPs etc).
  • Partner with safety and non-safety functions in regional/global projects to provide expertise and contribution.
  • Support CSLs to engage the PCO network.
  • Uses knowledge of industry, customer requirements and general business environment to adapt and implement strategic actions.
  • Exhibits a high level of business knowledge and understanding of the external marketplace, business line or other internal business partners' requirements.
  • Champions innovation and compliance.
  • Develops and leverages resources to implement innovative ideas, processes, across Cluster.
  • Consider thoughtful risks to achieve results without compromising regulatory compliance.
Requirements:
  • Management of ex-country units.
  • Good understanding of computer technology and demonstrated computer literacy particularly in use and management of relational databases.
  • Knowledgeable in pharmacovigilance regulations and requirements.
  • Knowledgeable in pharmaceutical business, including drug development and regulatory aspects.
  • Good understanding of medical and scientific terminology in both local language and English.
  • English Proficiency.
  • Knowledge and understanding of quality aspects, processes, audit, and inspections.
Qualifications:
  • Degree / Advanced degree in medicine or in life sciences or equivalent experience.
  • Several years of experience in the pharmaceutical industry in pharmacovigilance or clinical research or product development.
  • Rational approach to issues and their business implications.
  • Good problem solving and decision-making skills.
  • Team building and team management experience.
  • Strong interpersonal skills, with a demonstrated ability to manage people and foster teamwork.
  • Excellent communication and negotiation skills - ability to manage discussions and decision making across cultures.
  • Highly skilled in time management and change management, organizational and facilitation skills.
  • Ability to meet personal objectives while meeting departmental standards of performance.
  • Comfortable working in a matrix environment.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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