Senior Associate Senior Data Manager Clinical Data Sciences

Pfizer; Chennai District; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Pfizer Worldwide Medical and Safety teams support evidence-based medical decisions to improve patient outcomes. This Senior Associate Data Manager role focuses on data management plans, including data preparation, validation, and cross-team collaboration across clinical trials.

You will own data monitoring and management activities, ensure data quality via listings and reports, and help share lessons learned to drive operational excellence globally.

Qualifications

• Bachelor's Degree and 8+ years of data management experience.
• Knowledge of data management processes and principles.
• Experience with web-based data management systems.
• Working knowledge of electronic document management systems.
• Familiarity with ICH GCP and clinical study management processes.
• Strong time management and prioritization abilities.
• Excellent verbal and written communication skills.

Responsibilities

• Serve as Data Manager for one or more clinical trials.
• Ensure data monitoring and management deliverables with partners.
• Develop data cleaning reports to support the data review plan.
• Set up data review listings to verify data quality and completeness.
• Document lessons learned and share across study teams.
• Build relationships with SMEs across fields to identify solutions.

Skills

Data management

Data cleaning

Data review

Time management

Verbal and written communication

ICH-GCP familiarity

Education

Bachelor's Degree

Master's degree

Job description

Job Description

Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

What You Will Achieve

It is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility. You will play an important role in processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. You will ensure that accurate, timely, and consistent data reaches the clinical teams and other groups. You will be relied on for data management plans, including data preparation and validation activities, among others.

As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.

It is your commitment and hard work that will help make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Manage own time to meet agreed targets; develop plans for work activities on own projects within a team.
• Serve as Data Manager for one or more clinical trials assuming responsibility for Data Monitoring and Management (DMM) activities.
• Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan.
• Ensure operational excellence across all Data Monitoring and Management (DMM) deliverables.
• Set-up and test data review listings to verify the quality and completeness of data as specified in Data Management Plan by reviewing data attributes populated by general users.
• Ensure lessons learnt during the study are documented and shared with other study teams to facilitate cross-study learning.
• Build good relationships with local and global SMEs from different fields, leverage their expertise in areas such as systems and process and proactively identify issues and work to create solutions.

Qualifications

Must-Have

• Bachelor's Degree
• 8+ years’ experience
• Demonstrated knowledge of data management processes and principles
• Experience with web based data management systems
• Working knowledge of electronic document management systems
• Knowledge of International Conference on Harmonization and more specifically Good Clinical Practices
• Thorough understanding of the processes associated with clinical study management and regulatory operations
• Ability to manage tasks, time and priorities
• Demonstrated effective verbal and written communication skills and adapt communications to audience

Nice-to-Have

• 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

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.

Medical