Senior Associate, Senior Data Manager, Clinical Data Sciences

Pfizer Inc; Chennai; Hybrid; INR 900,000 - 1,500,000; Full time

Job summary

Pfizer Inc in Chennai, India seeks a Senior Data Manager in Clinical Data Sciences to oversee data cleaning, monitoring, and practical data management for clinical trials. This role emphasizes collaboration with global teams and maintaining high-quality deliverables.

The ideal candidate has 2+ years in data management with knowledge of ICH-GCP, EDMs, and EDC systems, and strong communication skills to document learnings across studies.

Qualifications

• Bachelor's or higher in a relevant field.
• Understanding of data management processes and principles.
• Experience with web-based data management systems and EDC.
• Familiarity with ICH-GCP guidelines and regulatory operations.

Responsibilities

• Contribute to moderately complex clinical data projects and manage short-term work plans.
• Serve as Data Manager for clinical trials, overseeing DMM activities.
• Collaborate with partners to ensure operational excellence and maintain data quality as per DM Plan.
• Document and share lessons learned across studies for cross-study learning.
• Engage with SMEs to leverage expertise in systems and processes.

Skills

Data management

Web-based DMS

ICH-GCP/regulatory

Communication skills

Clinical study management

Documentation systems

Analytical thinking

Education

BA/BS

MBA/MS

Tools

EDC systems

Data visualization tools

Job description

Senior Associate, Senior Data Manager, Clinical Data Sciences### Senior Associate, Senior Data Manager, Clinical Data SciencesApply: India - Chennai: Full time: Posted Today: 4967773**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.