As an experienced professional in Medical Affairs, you will oversee the direction, planning, execution, clinical trials/research, and data collection activities
Job Summary
As an experienced professional in Medical Affairs, you will oversee the direction, planning, execution, clinical trials/research, and data collection activities.
You will contribute to the implementation of clinical protocols, facilitate final reports, recruit clinical investigators, and negotiate study design and costs.
Responsibilities include directing human clinical trials (phases III & IV), participating in adverse event reporting and safety monitoring, and coordinating reporting information for regulatory agencies.
Matching Summary
As an experienced professional in Medical Affairs, you will oversee the direction, planning, execution, clinical trials/research, and data collection activities.