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.

As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.

It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them.

Primary Responsibilities

• 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.

• Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation.

• Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database.

• Determine reportability of scheduled reports, ensuring adherence to regulatory requirements.

• Consistently apply regulatory requirements and Pfizer policies.

• Participate, as appropriate, in local, internal, and external safety activities.

Technical Skill Requirements

• Experience in pharmacovigilance and/or data management preferred but not required.

• Experience and skill with medical writing an advantage.

• Demonstrated computer literacy.

• Experience in use and management of relational databases preferred.

Other job details

• Work Location Assignment:On-site 2-3x/week or as needed by the business;

• Last day to apply for job: November 6th, 2024.

EEO (Equal Employment Opportunity) & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.