of cumulative safety data with the safety risk lead. Monitor study safety issues and provide input to serious adverse events (SAEs... of clinical research to lead global clinical research programs and registration activities across one or more clinical projects...
Pfizerof individual subject safety data, and performs review of cumulative safety data with the safety risk lead. As appropriate, the... expertise and oversight for Clinical Trials and serves as a single point of accountability for design, execution, monitoring...
Pfizer