Main Responsibilities:
Antimicrobial & Antifungal Stewardship (AMS & AFS): Advocate for the rational
use of antimicrobial agents in clinical practice by optimizing AMS and AFS
systems and generating relevant medical evidence.
- Develop and refine AMS/AFS strategies in alignment with national and
regional antimicrobial management policies, guidelines, and data from
antimicrobial surveillance networks.
- Investigate the clinical use of antimicrobial agents through real-world
data, assess the impact of AMS/AFS strategies on patient outcomes, disease
management, and healthcare costs, and provide evidence-based support for the
rational of antimicrobials.
- Optimize AMS/AFS strategies to various clinical scenarios based on
real-world evidence, aiming to enhance the quality of antimicrobial application
and reduce the risk of resistance.
Quality Improvement (QI) in Antimicrobial Clinical Application: Identify and
address common challenges in the clinical use of antimicrobial agents by
analyzing relevant diagnostic and therapeutic processes to highlight
significant issues and propose constructive solutions to improve the quality of
antimicrobial application.
- Understand the standards in the diagnosis and treatment of infectious
diseases (ID), and develop and optimize QI strategies for the clinical
application of antimicrobial agents based on unmet needs, ensuring that the
standards align with advancements in the field of ID and meet clinical
requirements.
- Evaluate the effectiveness of antimicrobial clinical applications based on
the implementation of QI strategies, and conduct regular assessments to ensure
the sustainability of quality improvement measures.
- Integrate the resources in the ID field to create a comprehensive medical
activity platform that enhances academic influence and resource sharing.
- Monitor national healthcare policies, including Value-Based Purchasing (VBP)
and Diagnosis-Related Groups (DRG), and provide necessary medical support in
the field of infections as required.
ID products Lifecycle Management: Provide comprehensive medical support for
both early- and late-stage infection products, ensuring the medical guidance
and support are available at all stages of the product lifecycle to promote
product development.
- Support BD assessments in ID field, ensuring scientific validity of product
assessment.
- Prepare for and provide medical support for ID products that are over 3
years from commercial launch, establishing a foundation for successful product
launches.
- Provide necessary medical support as needed for late-stage infection
products, such as CSO products.
Required skills
Must-possess:
- Therapeutic area knowledge: familiar with the disease knowledge and clinical
practice of the therapeutic area
- Quick Learning: Ability to master advancements in the global medical field.
- Project Management: Demonstrated ability to manage projects effectively,
including proactive planning, resource coordination, risk management, and
ensuring high-quality outcomes.
- Efficient Execution: Capacity to quickly grasp task requirements and
effectively address implementation challenges.
- Interpersonal Communication: Strong communication skills to engage
effectively with diverse stakeholders at various levels.
- Strategic Thinking: Ability to think strategically and analyze complex
situations critically.
- Team Collaboration: A collaborative spirit with a commitment to working
effectively within a team.
- Language Proficiency: Fluent in English (both spoken and written) is
essential.
Preferred:
- Clinical Trial Knowledge: Basic understanding of clinical trial processes.
- Customer Orientation: A strong focus on meeting customer needs and
delivering high-quality medical services.
- Business Acumen: possess strong business insight
Educational Background:
Master degree or above in medicine, pharmacology or relevant therapeutic area.
Work Experience:
- Experience as a clinical physician.
- Minimum of 2 years of experience in the pharmaceuticals.
Previous Experience in medical affairs is preferred.


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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