Pfizer

Senior Associate, Data Manager, Clinical Data Sciences

Posted Yesterday

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Mumbai, Maharashtra, IND

Hybrid

Senior 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 monitoring and management activities, ensuring data quality, completeness, regulatory compliance, and adherence to data management plans. Develop data cleaning reports, coordinate with internal and global subject matter experts, identify and resolve operational issues, document lessons learned, and contribute to clinical study management projects.

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:

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

Skills Required

BA/BS degree with at least 2 years of experience, or MBA/MS degree with any years of experience
Knowledge of data management processes and principles
Proficiency in 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 using data visualization tools
Experience using 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 and understanding of responsible AI practices

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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.