Pfizer is looking to support healthcare decisions that ensure the safe and effective use of medications by developing frameworks for scientifically robust evidence, providing unbiased medical expertise, and bridging data gaps to improve patient care and treatment efficacy.
Requirements
- 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
- Experience using data visualization tools
- Proficient experience using commercial clinical data management systems and/or EDC products
Responsibilities
- 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.
Other
- Contribute to moderately complex projects, managing time effectively to meet targets and develop short-term work plans.
- BA/BS with at least 2 years of experience or MBA/MS with any years of experience
- Relevant pharmaceutical industry experience
- Effective verbal and written communication skills
- Ability to work collaboratively in a team environment
- Excellent organizational and time management skills
