Fortrea

Job Overview: Calling Clinical Data Managers / Database designers with strong experience in protocol interpretaion and edit checks specification keen to be trained in programming! Performs programming

Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s

Job Overview: It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. The individua

Job Overview: It is the responsibility of the postholder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. They will be e

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

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

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

Job Overview: May support LDM with the review, maintenance and update of External Vendor data received from central vendor or local laboratories. Working to ensure departmental SOPs, guidelines and gl

Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes ass

Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical t