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The Role
Perform clinical data monitoring and management activities: data review, query management, investigate logic checks, and ensure database design quality through documentation, testing, validation, and implementation of data collection tools. Act as first point of contact for CTMS issues, follow SOPs, collaborate to resolve TMF/document discrepancies, and contribute to process improvements and project work.
Summary Generated by Built In
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
Here Is What You Need (Minimum Requirements):
Bonus Points If You Have (Preferred Requirements):
Work Location Assignment: Hybrid
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 .
Medical
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
Work Location Assignment: Hybrid
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 .
Medical
Skills Required
- BA/BS degree
- Demonstrated experience with ICH/GCP documentation requirements
- Hands-on experience with electronic documentation management systems and/or web-based data management systems
- Awareness of the clinical development process and principles of Good Clinical Practice
- Understanding of regulatory requirements and relevant data standards
- Strong oral and written English communication skills
- Proficiency in Microsoft Office Suite
- 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 AI tools (e.g., ChatGPT, Microsoft Copilot) and understanding of responsible AI practices
What the Team is Saying
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Diagnostics Launch Lead
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R&D Privacy Steward
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Specialist
Pfizer
Pfizer Compensation & Benefits Highlights
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Healthcare Strength — Multiple U.S. medical plan options include telehealth, comprehensive mental‑health support, fertility/family‑building benefits, transgender‑inclusive coverage, and certain Pfizer medications at no cost. A Wellbeing Wallet and wellness resources broaden the health and wellbeing offering.
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Retirement Support — A 401(k) with company matching is paired with an additional Pfizer Retirement Savings Contribution, alongside company‑paid life and disability insurance. One‑on‑one financial planning support is provided through Fidelity.
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Leave & Time Off Breadth — Paid time off spans vacation, holidays, and personal days, with additional caregiver and medical leave. U.S. parental leave commonly includes 12 weeks paid with options for additional unpaid bonding time and a return‑to‑work transition.
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The Company
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Typical time on-site:
2.5 days a week
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