Senior Associate, Senior Data Manager Clinical Data Sciences

Posted 7 Hours Ago
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Mumbai, Maharashtra
Hybrid
Junior
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
As a Senior Associate, Senior Data Manager, you will oversee data management activities for clinical trials, ensure data quality, collaborate with teams, and document lessons learned. You will also manage projects, maintain DMM standards, and identify solutions to data-related challenges.
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


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.
Medical
#LI-PFE

What the Team is Saying

Daniel
Anna
Esteban
The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
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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