As a Senior Associate, you will support Pfizer’s commitment to ensuring the accuracy, visibility, and quality of clinical data. Your contributions will strengthen oversight in clinical data management processes, driving operational excellence.
Key responsibilities include:
- Serving as the Data Manager for one or more clinical trials.
- Managing Data Monitoring and Management (DMM) activities.
- Developing and implementing Data Management Plans to validate and review clinical data.
- Testing and verifying data review listings to ensure quality and completeness.
- Collaborating with internal and external stakeholders to maintain operational excellence.
- Documenting lessons learned and sharing best practices to enhance cross-study learning.
Qualifications
Must-Have:
- Bachelor’s Degree in a relevant field.
- At least 8 years of experience in data management processes.
- Demonstrated expertise with web-based data management systems.
- Working knowledge of electronic document management systems.
- Familiarity with International Conference on Harmonization (ICH) and Good Clinical Practices (GCP).
- Strong understanding of clinical study management and regulatory operations.
- Excellent time management and communication skills.
Nice-to-Have:
- Master’s Degree or advanced qualifications.
- Relevant pharmaceutical industry experience.
- Proficiency in using data visualization tools.
- Experience with commercial clinical data management systems or EDC products.
- Awareness of regulatory requirements and data standards.
Key Skills Required
- Data Management Expertise
- Knowledge of ICH and GCP Standards
- Strong Analytical and Problem-Solving Abilities
- Proficiency in Web-Based and Electronic Systems
- Effective Communication and Collaboration
