Senior Associate, Data Manager, Clinical Data Sciences

Posted 2 Hours Ago
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Mumbai, Maharashtra, IND
In-Office
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
Serve as Data Manager for clinical trials, oversee data monitoring and management activities, ensure data quality and completeness per the Data Management Plan, produce data cleaning reports, collaborate with global SMEs, document lessons learned, and support operational excellence across DMM deliverables.
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

Skills Required

  • 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 ICH Good Clinical Practice (GCP)
  • 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
  • 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

What the Team is Saying

Daniel
Anna
Esteban
Pfizer

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.

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Pfizer Offices

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Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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