Associate Medical Manager I
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
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Med Data Review Assoc Mgr
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
Project Manager Drug Safety
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
Centralized Study Analyst
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
Central Monitor Assistant
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
Clinical Research Associate II
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
Safety Systems Specialist
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
Senior Analyst, Real World Evidence
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
Central Monitoring Associate Manager
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
Biostatistician I
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
Associate Validator II
Job Overview: Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scan
Associate Clinical Data Manager (External Data)
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
Associate Clinical Data Manager
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
REGULATORY AND START-UP
Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with s
Regulatory Manager
Job Overview: Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and acc
Manager, Business Intelligence
The Manager, Business Intelligence leads and develops a team of Commercial analysts responsible for delivering high-quality reporting, dashboards, and data-driven insights that support business dec
Safety Systems Associate II, PSS
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
Site Engagement Lead
Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the P
Principal Biostatistican
Summary of Responsibilities: Lead complex studies such as NDA submissions or complex, multi-protocol programs, potentially coordinating activities across multiple locations, providing statistical over
Centralised Clinical Team Lead
Summary of Responsibilities: Management of complex projects under the direction of a Project Manager/Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted acco
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