You are entrusted to fulfil the following responsibilities:
- You will be responsible for performing various tasks related to Testing and Validation.
- Responsible for performing testing of inform build (eCRF screens, edit checks and related aspects of EDC to CDMS systems) systems before production go-live to ensure smooth data flow and transformations.
- Furthermore, you will have basic understanding about the systems like, EDC, DMW and related interfaces.
- Additionally, you will be providing detailed description of scenarios that failed in UAT plan and report. In addition to this, you will suggest additional test scenario to be added to the Test Plan.
- You will communicate suggestions or concerns regarding testing with relevant Clinical Data Programmer-EDC.
Qualification:
- MSc / BSc in Life Science or comparable degree in computer science, Information Technology clinical information management or equivalent qualifications.
- 3+ years of experience in pharmaceutical industry and preferably 1 years within clinical systems.
- Minimum 1-2 years of experience in pharmaceutical industry and preferably 1 years within clinical systems.
- Good knowledge of GxP guidelines within drug development.
- Understanding the variances of clinical data types.
- Understanding the specifications.
- Regular experience with communication and presentations.
- Personality with team spirit & Self-motivated.
