Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work workplace. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us.
Responsibilities will include, but are not limited to
Study Startup
Draft EDC build timeline in collaboration with Data Management Lead.
Perform DB build tasks by creating specifications for Database and Edit Checks.
Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway.
Collaborate with Data Management Lead and facilitate startup meetings which includes, not limited to, EDC build kick-off, Interactive eCRF Build and IRMs (Interactive Review Meeting) for database and Edit checks.
Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP) post study team review.
Ensure all startup documents are completed as per SOP and filled in eTMF as per eTMF master plan.
Study Conduct
Plan/execute Post-Production/Migration for the study (if any).
Coordinate with Clinical Data Managers for the execution of data review tasks.
Coordinate with external data vendors for any escalations related to any vendor data.
Support Clean Patient Group delivery along with Clinical