Fortrea

Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the postmarketing period; and may manage a team. Summary of Respons

Job Overview: The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the C

Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials an

Summary of Responsibilities: To complete other duties/activities as assigned by study management team, but not limited to: Manage clinical systems and access management. Manage study documents and sup

Summary of Responsibilities: To complete Other duties/activities as assigned by study management team, but not limited to: Manage clinical systems and access management. Maintain study databases (CTMS

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirem

Job Overview: Assist with the overall safety system implementation, support, configuration, and migration related activities. Responsible for providing this service to clients either as a support func

Job Overview: Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the ana

Job Overview: Reviews trip reports, proactively identifies risks and communicate any trends, outstanding issues, safety concerns to the study team. Responsible for the execution of key Central monitor

Summary of Responsibilities: For Clinical Pharmacology studies, perform role of Lead Biostatistician. For Clinical Pharmacology studies, maintain awareness of project budgets and tasks. Assist in the