Why Patients Need You

Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

What You Will Achieve

You will be relied on by the company to monitor its drug, biologics and medical devices surveillance program. This will include intake, evaluation and processing of the adverse reports received. You will support the clinical trial as well as the post marketing activities.

• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
• Provide oversight, team mentoring on case handling aspects, data extraction and analyses and conduct follow-up activities.
• Act as subject matter expert and liaise with key partners regarding safety data collection and data reconciliation.
• Review, analyze, prepare, and complete safety-related reports within scope to determine the safety profile of Pfizer's products and to meet regulatory requirements.
• Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.
• Manage, where applicable, safety resources in the local team.
• Provide specific pharmacovigilance or product knowledge and experience, as required by the business, and mentor colleagues accordingly.
• Develop and maintain advanced knowledge of all products within the Pfizer portfolio.
• Develop and maintain expertise of all assigned products, of applicable corporate policies.
• Design and oversee the tracking of applicable safety metrics.
• Manage project and process management meeting established deadlines.
• And search functions in the safety database and data mart.
• Participate, as appropriate, in local, internal and external safety activities
• Carry out case processing activities
• Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments
• Review case criteria to determine appropriate workflow for case processing
• Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately
• Write and edit case narrative
• Determine and perform appropriate case follow-up, including generation of follow-up requests
• Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios

• Bachelor's Degree
• Pharmacist
• 3+ years' experience
• Demonstrated organizational/project management skills
• Solid knowledge of global regulations and guidelines for drug development
• Demonstrated analytical and statistical skill.
• Ability to make decisions independently and resolve issues appropriately
• Strong skills in productivity, organizational and time management in order to meet strict regulatory compliance goals
• Fluent in spoken and written English

• Master's degree
• Relevant pharmaceutical industry experience
• Familiarity with management of performance metrics
• Ability to make decisions independently in both routine case processing and unique and/or complex situations, and to resolve issues appropriately to achieve a desired result or impact