Pfizer

Data Manager, Clinical Data Sciences

Posted 5 Hours Ago

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Buenos Aires, Ciudad Autónoma de Buenos Aires, ARG

In-Office

Entry level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Manage clinical trial data quality and integrity: perform data monitoring and query management, validate and test clinical data collection tools, support CTMS users, follow SOPs, resolve TMF/document discrepancies, and contribute to process improvements.

Summary Generated by Built In

Work Location Assignment: Buenos Aires, Argentina. Must be able to work from assigned Pfizer office 2-3 days per week, or as needed by the business
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

EEO (Equal Employment Opportunity) & Employment Eligibility
Pfizer is 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 gender expression, national origin, or disability.
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
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 Good Clinical Practice principles
Solid grasp 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

Pfizer Compensation & Benefits Highlights

Healthcare Strength — Health coverage includes comprehensive medical with robust mental‑health networks, plus dental and vision options, and coverage for infertility/family‑building and transgender‑affirming care. Recent U.S. summaries name mental‑health partners and outline multiple plan choices.
Retirement Support — The retirement program provides a 401(k) with company match plus an additional employer Retirement Savings Contribution, along with financial‑planning support and company‑paid life and disability insurance. These elements are highlighted as part of the core U.S. package.
Parental & Family Support — Parental leave is described as up to 26 weeks in the U.S. when combining paid non‑medical parental leave with medical recovery where applicable, with exact pay and weeks dependent on circumstances and plan elections. Family‑building support includes egg preservation, adoption, and surrogacy coverage.

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

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.