Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.
What You Will Achieve
In this role, you will:
Coordinate and support all activities related to clinical trials, assisting managers in their execution.
Assist in site activation activities, including gathering necessary documentation.
Review data for quality and completeness, ensuring timely submission to data management and supporting patient safety and eligibility.
Coordinate with sites to finalize budget worksheets and contractual agreements, maintaining accurate site-level information on the clinical trials registry.
Support the study team with regulatory submissions, maintain the Electronic Library and Records Archive, and attend investigator meetings as required.
Here Is What You Need (Minimum Requirements)
BA/BS with at least 2 years of experience or MBA/MS with any years of experience
Demonstrated success in prior roles, including within matrix organizations
Deep understanding of quality and regulatory requirements across various countries
Knowledge of International Conference on Harmonization Good Clinical Practices and local regulations
Proficiency in applications used in clinical trials
SOP compliance knowledge and expertise on all relevant SOPs
Effective verbal and written communication skills, and fluency in English
Bonus Points If You Have (Preferred Requirements)
A Master's degree combined with relevant therapeutic area experience
High level of project management skills
Strong analytical and problem-solving skills
Ability to work independently and as part of a team
Excellent organizational and time management skills
Strong attention to detail
Proficiency in Microsoft SharePoint and SharePoint Designer
Ability to adapt to changing priorities and work in a fast-paced environment
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.
