Medical Affairs Specialist at Abbott

Oversee the direction, planning, execution, clinical trials, research, and data collection activities within the Medical Affairs Sub-Function

Contribute to the implementation of clinical protocols and facilitate the completion of final reports

Recruit clinical investigators and negotiate study design and costs

Direct human clinical trials, phases III and IV for company products under development

Participate in adverse event reporting and safety responsibilities monitoring

Coordinate and provide reporting information for reports submitted to regulatory agencies

Monitor adherence to protocols and determine study completion

Coordinate and oversee investigator initiations and group studies

Abbott