Manager, Clinical Data Management - Pfizer
About the Opportunity:
Pfizer Worldwide Medical and Safety teams are essential in connecting evidence-based medical decision support with colleagues and stakeholders, ultimately enabling better health and treatment outcomes. As a Manager in Clinical Data Management, you will play a pivotal role in overseeing clinical data processes, ensuring accurate, timely, and consistent delivery of data that is vital to advancing healthcare decisions. This is an opportunity to contribute to groundbreaking work that improves patient outcomes globally.
What You Will Achieve:
As a Manager, Clinical Data Management, your responsibilities will include:
Leadership & Project Management: Provide guidance and lead projects, managing your own time to meet objectives and ensuring resource requirements for projects are effectively planned.
Data Management Expertise: Oversee all Data Monitoring and Management (DMM) activities for clinical trials. Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials, ensuring data integrity and high-quality deliverables.
Collaboration & Technical Support: Work closely with research/business units, external data management service providers, and study teams to ensure seamless data acquisition, proactive data review, and operational excellence.
Central Monitoring: Conduct central monitoring activities, review system outputs, and manage actions for data signal and integrity issues. Provide actionable insights and resolutions to study teams.
Process Improvement: Drive the application of consistent, efficient processes, promote the use of data visualization and reporting tools, and contribute to the continuous improvement of clinical data management practices.
Communication & Engagement: Lead communication plans, engaging stakeholders and ensuring alignment across teams and customers.
Qualifications:
Must-Have:
Education: Bachelor’s Degree in a relevant field.
Experience: 5+ years of experience in the pharmaceutical industry or health information management.
Knowledge: Strong understanding of all phases of clinical trials, GCDMP, FDA, ICH-GCP, and related regulatory requirements.
Project & Risk Management: Proven experience in managing projects, risks, and timelines effectively.
Skills: Excellent verbal and written communication skills, ability to manage multiple projects, and proficiency with Windows applications.
Nice-to-Have:
Education: Master’s degree.
Experience: Experience in Contract Research Organization (CRO) and vendor oversight.
Technical Skills: Proficiency in commercial clinical data management systems or EDC products.
Work Location:
On Premise
Why Pfizer:
Pfizer is an equal opportunity employer, committed to diversity and inclusion. We comply with all applicable equal employment opportunity legislation in the jurisdictions we operate in. Join us to help make a difference for patients worldwide.
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