About the job
Job Description
We are seeking a dedicated and skilled Clinical Trial Medical Monitor to join our team, focusing on oncology studies. You will collaborate with the Clinical Trial Lead, Program Lead, or Early Asset Development Lead, along with a cross-functional study team, to ensure the integrity of ongoing clinical trials and facilitate database locks.
Key Responsibilities
- Monitor and clean ongoing oncology studies.
- Review safety data with clinical teams using tools such as J-Review, CIOMS, and CFR imaging tools.
- Attend weekly update meetings with the BMS core team (PM, DM, stats, CRO) as necessary.
- Respond to inquiries from sites and Health Authorities regarding the protocol.
- Conduct weekly investigator calls for Phase I studies as needed.
- Review monthly safety data and protocol deviations, and communicate with CRO sites regarding follow-up actions.
- Participate in monthly safety meetings and review daily lab alerts and SAEs.
- Design and implement comprehensive safety monitoring plans.

