Clinical Trial Hub Safety Specialist
hace 2 semanas
Pfizer's mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. As a key member of our team, you will play a vital role in monitoring our drug, biologics, and medical devices surveillance program.
This includes intake, evaluation, and processing of adverse reports received. You will support clinical trials as well as post-marketing activities. Your expertise and knowledge will contribute towards the goals and objectives of the team, helping us achieve our mission.
To succeed in this role, you will need strong organizational and project management skills, solid knowledge of global regulations and guidelines for drug development, and demonstrated analytical and statistical skill. Additionally, you must be able to make decisions independently and resolve issues appropriately.
You will be responsible for reviewing, analyzing, preparing, and completing safety-related reports within scope to determine the safety profile of Pfizer's products and meet regulatory requirements. This will involve managing safety resources, mentoring colleagues, developing advanced knowledge of all products within the Pfizer portfolio, and maintaining expertise on assigned products.
We are 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 expression, national origin, or disability.
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