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Manager, Project Manager, Clinical Database Management, DMM
2 weeks ago
Why Patients Need You
Pfizer Worldwide Medical and Safety colleagues play a crucial role in connecting evidence-based medical decision support with colleagues and stakeholders to enhance health and treatment outcomes. Whether you are establishing frameworks to ensure the scientific validity of our evidence, offering impartial and medically necessary expertise, or exploring ways to address data gaps, our goal remains simple: Empower healthcare decisions for the safe and proper use of medications by patients.
What You Will Achieve
Our mission is to enhance the oversight of our clinical data by strengthening ownership, control, and visibility. In this role, you will be pivotal in processing, reviewing, and managing patient data and records, organizing clinical data forms, and ensuring the accuracy and timeliness of clinical data reaching various departments. Your responsibilities will include developing data management plans, overseeing data preparation, and validation activities.
As a Manager, you will provide guidance to operational teams, assist in project management, and contribute to resource forecasts and process improvements. Your expertise will be instrumental in advancing new concepts and methodologies while fostering collaboration between different teams.
Your dedication and focus will prepare Pfizer to reach new milestones and support patients globally.
How You Will Achieve It
- Provide guidance and leadership on projects, manage time effectively to meet objectives, and plan resource allocations.
- Ensure adherence to Standard Operating Procedures and promote efficient processes.
- Act as a Clinical Data Scientist and Trial Lead, overseeing Data Monitoring and Management (DMM) activities.
- Offer technical support for data visualization and reporting tools, ensuring data integrity and operational excellence.
- Collaborate with partners and external service providers to maintain high-quality data management.
- Conduct central monitoring activities, propose action plans, and drive resolutions with study teams.
- Develop communication strategies for engaging customer populations.
Qualifications
Must-Have
- Bachelor's Degree
- 5+ years of experience
- Experience in the pharmaceutical industry or health information management
- Knowledge of clinical trials, FDA & GCDMP regulations, and strong Project and Risk Management skills
- Effective verbal and written communication, ability to manage multiple tasks, and proficiency in Windows Environment
Nice-to-Have
- Master's degree
- Experience in Contract Research Organization (CRO) and vendor oversight
- Proficiency in clinical data management systems/an EDC products
Location: On-Site
Pfizer is an equal opportunity employer and adheres to all relevant equal employment opportunity laws in its operating jurisdictions.
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