Use Your Power for Purpose
At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. You will play a crucial role in improving patients' lives by ensuring the accuracy and integrity of clinical data. Your work will directly impact the development of new treatments and therapies, helping to bring innovative solutions to patients in need.
What You Will Achieve
•Engage in Data Monitoring and Management (DMM) activities, including data review, query management, and investigating logic check flags.
•Ensure the quality of database design through documentation, testing, validation, and implementation of clinical data collection tools or systems.
•Serve as the first Point of Contact for customers needing assistance with Clinical Trial Management System (CTMS) questions and issues.
•Adhere to applicable Standard Operating Procedures (SOPs) and working practices.
•Collaborate with Study Team Points of Contact, Document Owners, and Trial Master File (TMF) Study Owners to resolve document-related discrepancies and issues.
•Contribute to process improvement initiatives and additional projects as they arise.
Here Is What You Need (Minimum Requirements)
•BA/BS with any years of experience
•Demonstrated experience of ICH/GCP (International Council for Harmonization/Good Clinical Practice) documentation requirements
•Hands-on experience with electronic documentation management systems and/or web-based data management systems
•Awareness of the clinical development process, including a deep understanding of the principles of Good Clinical Practice
•Solid grasp of regulatory requirements and relevant data standards
•Strong oral and written English communication skills
•Proficiency in Microsoft Office Suite
Bonus Points If You Have (Preferred Requirements)
•Experience with clinical trial management systems (CTMS)
•Familiarity with data validation and quality control processes
•Ability to work collaboratively in a team environment
•Strong problem-solving skills and attention to detail
•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
Please apply by sending your CV in English.
Work Location Assignment: Hybrid
This role is posted in multiple locations. If you are applying for the role in a secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.
