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We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Manage clinical trial data monitoring and management activities, including data cleaning, quality control, completeness, and adherence to Data Management Plans. Collaborate with global subject matter experts and study partners, develop work plans, document lessons learned, and resolve operational issues. The role requires knowledge of clinical data management processes, regulatory operations, ICH Good Clinical Practice, electronic systems, and clinical study management.
Summary Generated by Built In
Use Your Power for Purpose
Our mission is straightforward: support healthcare decisions that ensure the safe and effective use of medications. 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:
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
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.
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
Our mission is straightforward: support healthcare decisions that ensure the safe and effective use of medications. 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:
- Contribute to moderately complex projects, managing time effectively to meet targets and develop short-term work plans.
- Take on the role of Data Manager for clinical trials, overseeing Data Monitoring and Management (DMM) activities.
- Collaborate with partners and colleagues to ensure operational excellence and apply standards while developing data cleaning reports.
- Maintain high standards across all DMM deliverables and ensure data quality and completeness as specified in the Data Management Plan.
- Document and share lessons learned during studies to promote cross-study learning.
- Build strong relationships with local and global subject matter experts (SMEs) to leverage their expertise in systems and processes, proactively identifying issues and developing solutions.
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 knowledge of data management processes and principles
- Proficiency in web-based data management systems
- Working knowledge of electronic document management systems
- Familiarity with the International Conference on Harmonization, particularly Good Clinical Practices
- Thorough understanding of clinical study management and regulatory operations processes
- Effective verbal and written communication skills
Bonus Points If You Have (Preferred Requirements)
- Master's degree
- Relevant pharmaceutical industry experience
- Experience using data visualization tools
- Proficient experience using commercial clinical data management systems and/or EDC products
- Awareness of regulatory requirements and relevant data standards
- Strong analytical and problem-solving skills
- Ability to work collaboratively in a team environment
- Excellent organizational and time management skills
- 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: On Premise
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 or BS degree with at least 2 years of experience, or MBA or MS degree with any years of experience
- Knowledge of data management processes and principles
- Proficiency with web-based data management systems
- Working knowledge of electronic document management systems
- Familiarity with International Conference on Harmonization Good Clinical Practices
- Understanding of clinical study management and regulatory operations processes
- Effective verbal and written communication skills
- Master's degree
- Relevant pharmaceutical industry experience
- Experience with data visualization tools
- Experience with commercial clinical data management systems or EDC products
- Awareness of regulatory requirements and relevant data standards
- Strong analytical and problem-solving skills
- Ability to work collaboratively in a team environment
- Excellent organizational and time management skills
- Experience using generative AI tools such as ChatGPT or Microsoft Copilot, with awareness of responsible AI practices
What the Team is Saying
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Diagnostics Launch Lead
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R&D Privacy Steward
Esteban
Specialist
Pfizer
Pfizer Compensation & Benefits Highlights
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Healthcare Strength — Health coverage is described as comprehensive across medical, dental, vision, and mental‑health support, with strong plan options and provider networks. Feedback suggests these programs are a clear standout within the total rewards package.
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Retirement Support — Retirement programs feature a 401(k) with company matching plus an additional company retirement contribution. Feedback suggests these elements are consistently highlighted as valuable components of overall compensation.
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Leave & Time Off Breadth — Paid vacation, holidays, and sick time are often characterized as generous, with some locations offering the ability to purchase additional vacation days. Feedback suggests this breadth contributes meaningfully to work‑life balance.
Pfizer Insights
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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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