Life Science : SAS Programmer : CDB Programmer : Apply

Role & responsibilities :

1.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans.

2. Develop library of reusable checks working closely with data engineers and config specialists.

3. Collaborate with cross functional teams in creating business rules and automated check

library across TAU.

4. Serves as a technical resource for creating data analytics to help with data validation and cleaning.

5. Provide programming expertise for data cleaning to efficiently ensure high quality data.

6. Ensure accurate delivery by creating macros for Standard listings for the department based on specifications.

7. Develop programs that generate CRF and Query metrics, including ad-hoc Sponsor and

internal programming requests.

8. Ability to set up and configure analytics for coding reports, safety review and any risk-based monitoring activities.

9. Operational experience in pharmaceutical drug development with significant direct exposure to clinical

development and data operations required for the reporting of clinical trial data (e.g. data review, regulatory submissions, safety updates, etc.)

10. Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable

11. Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle),

12. EDC build and / or clinical data management experience preferred

13. Experience in AWS preferred

14. Experience setting up automated validation is preferred

15. Knowledge of Data lake and creating interactive Dashboards are preferred

16. Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)

Skills Required

Sql, Python