Senior Associate Data Manager

Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve

You will help oversee and execute the collection, curation, validation and processing of nonclinical data. Work with colleagues to develop and implement data management procedures, including data processing tools, business rules, and data entry guidelines. Support and facilitate the review of AI / ML derived data and medical coding for validity and completeness. Responsible for maintaining the highest data quality standards throughout the data lifecycle, from data collection to analysis. Stay updated on industry best practices, technological advancements and regulatory requirements related to nonclinical data management.

How You Will Achieve It

• Manage and perform data extraction, processing, curation, and formatting projects
• Create analysis ready data sets from multiple data sources, including documents (nonclinical study reports, articles, etc.)
• Collaborate with colleagues to provide data-related services including data collection, processing, preparation, and reporting
• Partner with stakeholders to generate insights through data visualizations and reports
• Ensure compliance with guidelines, Good Laboratory Practice (GLP), CDISC standards and other relevant regulations.
• Contribute to the development and validation of data management software tools 
• Troubleshoot data-related problems
• Assist in the development and implementation of strategies ensure data quality and completeness

Qualifications

Must-Have

• Bachelor’s degree in a scientific or healthcare-related field
• 1-3 years of experience working with biomedical information in a similar role in the pharmaceutical, medical or clinical research industry
• Ability to liaise successfully with project teams, including strong written and verbal communication skills
• Ability to successfully manage multiple tasks and timelines and perform assigned tasks with minimal supervision
• Proficient in Microsoft Excel

Nice-to-Have

• Knowledge of industry-standard data analysis and reporting software, such as R, SAS and/ or SQL
• Familiarity with GLP/GCP regulations
• Knowledge of CDISC standards and data interchange formats (e.g., SEND, SDTM, ADaM)

  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Research and Development

#LI-PFE