Anjana Chipurupally

1.Meeting project deadlines and deliverables for various Oncology studies, adhering to applicable Standard Operating Procedures (SOPs). 2.Understanding the expectations of stakeholders and negotiating internally and externally to ensure quality deliverables. 3.Participating in the development of standard library under the SDTM format. 4.Training new hires on study specific procedures and Data Management activities.

1.Defining, running, and reviewing edit checks and resolving discrepant data. 2.Independently issuing queries based on manual data review requirements for assigned studies. 3.Assisting in the management of the database cleaning and locking process. 4.Performing external data reconciliation under the direction of the Clinical Data Lead. 5.Specialized in Oncology trials with response criteria such as RECIST1.1, Clinical, Lugano, PCWG3, etc..

1.Work with Investigator Sites on Site Surveys and Site Qualification. 2.Perform established image processing techniques across multiple modalities such as CT, MRI, and X-Ray. 3.Monitoring within assigned projects of Good Clinical Practices (GCP), additional regulatory requirements (21 CFR Part 11), applicable departmental and company-wide SOPs, and project specific protocol compliance. 4.Providing administrative support to the Project Manager and project team.

Microbiology