Responsible for supporting the Pfizer Biopharmaceuticals Group EM Center of Excellence, specifically:

• Working collaboratively with Medical and Marketing teams to review promotional, regulatory, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
• Advocating best practices for achieving effective and complaint medical and promotional communications for Pfizer products
• Under supervision from line manager, ensuring that the operational deliverables of assigned deliverables are achieved on or ahead of schedule and within standards such that they meet the desired outcomes (i.e. quality standard, value)

• Uses scientific expertise and medical knowledge to ensure appropriate review of promotional, regulatory, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
• Liaises with all commercial functions in the review for scientific/ medical accuracy prior to and through the MLR review process as required
• Ensuring clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
• Collaborating with other lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned document

• Maintains the promotional material review process and system knowledge as per Pfizer standards
• Produces analytics reports and project scorecards as required in line with decided KPIs and sharing these with the line manager
• Collates team reports for each region to share with the medical team
• Monitors miletones, identifying potential risks and assisting in resolving any issues
• Conducts quality control assessments of assigned deliverables as required
• Faciliate creation of a robust feedback mechanism to ensure periodic inputs from stakeholders
• Under supervision from line manager, conduct training and onboarding of newly hired colleagues

• Prioritizes and multitasks to enhance productivity and manage workload
• Under supervision from line manager, communicates with stakeholders regarding project progress to cross functional teams and ensuring that quality standards are being met and to optimize efficiency

• Post-graduate degree in Pharmaceutical Science or graduate in Medical science (MBBS)
• Prior work experience as a member of Promotional and more medical/ scientific material review team

• Technical skills: Knowledge of "pharmaceutical medicine" including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant Therapeutic Area/Products
• Analytic skills: Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them. Analytical skills and reasoning, and sound medical judgment/decision making
• Regulatory knowledge: Familiarity with global regulatory guidance (especially ICH, FDA and EMA) relevant to clinical and safety data.
• Software: Previous experience with software commonly used to present and analyze data and experience with searching academic databases.(Word, PowerPoint, Excel) is preferred. Working knowledge of tools to aid the promotional material review process (GCMA/ Zinc/ PMAW) is required.