Manage clinical trial data monitoring and management activities, ensuring data quality, completeness, regulatory compliance, and adherence to data management plans. Develop data cleaning reports, collaborate with global subject matter experts, identify and resolve issues, maintain study deliverables, and document lessons learned. The role also supports operational excellence across clinical study management and regulatory processes.
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: 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
#BI-Hybrid
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: 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
#BI-Hybrid
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
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