- Perform activities, including but not limited to the testing of CRF design, Acquisition & Processing of electronic data, such as external eData, Lab Data and PK/PD Data, database edit checks under appropriate oversight.
- Accountable for high quality and on time delivery for assigned deliverables.
- Ensure the consistent use and application of applicable data standard and ensures data quality and consistency across programs and repositories.
- Ensure work carried out in accordance with applicable SOPs and working practices.
- Understand the Protocol to perform Screen testing.
- Participate in UAT feedback meetings.
- Track the lessons learned and share the knowledge across the team.
- Complete all the documentation related to study and share it with study Team.
- Awareness of clinical development and pharmaceuticals as a regulated industry
- Awareness of healthcare regulatory authorities (e.g., FDA, Health Canada)
- Ability to learn clinical data management processes and principles in area of responsibility.
- Demonstrates required verbal and written communication skills including ability to communicate remotely.
- Capable to learn technical data systems.
- Capable to learn how to use data visualization tools (e.g. Spotfire, J-Review)
- Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
- Bachelor’s degree minimum requirement. Health Sciences experience or Technology degree preferred.
- 0 to 1 year of relevant experience in Clinical domain / Life Sciences / Pharma.
- Knowledge and experience in functional / automation testing, SDLC, database management role, understanding key processes and principles associated with role including CRF design, database set-up, edit check specification, data transfer activities preferred.
Work Location Assignment: Flexible
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.