Senior Associate, Senior Data Manager, Clinical Data Sciences

Pfizer; Mumbai; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Pfizer in Mumbai seeks a Data Manager for clinical trials to oversee Data Monitoring and Management activities and ensure data quality across studies.

You will collaborate with local and global SMEs, maintain DMM deliverables, and develop data cleaning reports, while applying ICH/GCP standards and ensuring regulatory operations are met.

Qualifications

• BA/BS with at least 2 years of experience or MBA/MS 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 ICH, Good Clinical Practices (GCP).
• Understanding of clinical study management and regulatory operations processes.
• Excellent verbal and written communication skills.

Responsibilities

• Contribute to moderately complex projects, managing time effectively to meet targets and develop short-term work plans.
• Take on 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 SMEs to leverage their expertise in systems and processes, proactively identifying issues and developing solutions.

Skills

Data management

GCP familiarity

EDC platforms

EDMS

Communication skills

Education

BA/BS in related field

MBA/MS in related field

Tools

EDC platforms

EDMS

Job description

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

• 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.