Fortrea

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

About the RoleThis unique hybrid role blends the responsibilities of site startup site navigation and clinical monitoring. As a SCRA / Site Navigator II you will serve as a trusted partner to investigative sites across the full study lifecyclefrom feasibility and activation through mo

About the RoleThis unique hybrid role blends the responsibilities of site startup site navigation and clinical monitoring. As a SCRA / Site Navigator II you will serve as a trusted partner to investigative sites across the full study lifecyclefrom feasibility and activation through mo

*** Free parking ***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a RNs and LPNs to interact directly with our healthy volunteer participants while learning to read clini

*** Free parking ***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a RNs and LPNs to interact directly with our healthy volunteer participants while learning to read clini

Job Overview:The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned.Summary of Responsibilities:Segregate cases received as per priority and due dates in the database worklist.Assign cases to case processing t

Job Overview:The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned.Summary of Responsibilities:Segregate cases received as per priority and due dates in the database worklist.Assign cases to case processing t

Senior Clinical Data Manager Medical DeviceThe Senior Clinical Data Manager role is a great opportunity to work within our Medical Device Team and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management queries from being i

Senior Clinical Data Manager Medical DeviceThe Senior Clinical Data Manager role is a great opportunity to work within our Medical Device Team and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management queries from being i

What if your Pharmacy expertise was the reason a new drug reached patients fasterFortreas Clinical Research Unit in Leeds is a purposebuilt 65000 ft² Phase I facility where lifesaving medicines begin their journey.Here a modern clinic laboratory and cGMP research pharmacy sit under on

What if your Pharmacy expertise was the reason a new drug reached patients fasterFortreas Clinical Research Unit in Leeds is a purposebuilt 65000 ft² Phase I facility where lifesaving medicines begin their journey.Here a modern clinic laboratory and cGMP research pharmacy sit under on

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 trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp

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 trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp

Job Overview:Responsible for the analytical support for the developmental projects/comparative dissolution projects and for the proper recording of information.Summary of Responsibilities:Responsible to provide analytical support for the developmental projects/comparative dissolution

Job Overview:Responsible for the analytical support for the developmental projects/comparative dissolution projects and for the proper recording of information.Summary of Responsibilities:Responsible to provide analytical support for the developmental projects/comparative dissolution

Fortrea is looking for Senior Biostatistician to join our sponsor dedicated teamAs a Senior Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treatments. S

Fortrea is looking for Senior Biostatistician to join our sponsor dedicated teamAs a Senior Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treatments. S

Location: Poznań PolandWe are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development. Key Re

Location: Poznań PolandWe are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development. Key Re

Our FSO department in Portugal is looking for a CRA I / II to manage clinical studies principally in Oncology Hematology and Immunology . Home based in Porto area.Main Responsibilities: Clinical site monitoring: conducts routine prestudy initiation and closeout visits ensuring full co

Our FSO department in Portugal is looking for a CRA I / II to manage clinical studies principally in Oncology Hematology and Immunology . Home based in Porto area.Main Responsibilities: Clinical site monitoring: conducts routine prestudy initiation and closeout visits ensuring full co

Job Overview:The Embedded Technology Lead enables and accelerates clinical development delivery through the strategic and operational application of technology. Embedded within client programs or accounts this role serves as a trusted technology advisor and execution partner aligning

Job Overview:The Embedded Technology Lead enables and accelerates clinical development delivery through the strategic and operational application of technology. Embedded within client programs or accounts this role serves as a trusted technology advisor and execution partner aligning

Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.Key ResponsibilitiesConduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.Ensure patient safety data integrity and p

Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.Key ResponsibilitiesConduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.Ensure patient safety data integrity and p

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this r

Are you a proposal leader who thrives in a fastpaced clientdriven environmentsomeone who enjoys developing and supporting a highperforming team while remaining closely connected to complex strategic opportunitiesWe are hiring a Manager Proposal Management to join Fortreas Enterprise C

Are you a proposal leader who thrives in a fastpaced clientdriven environmentsomeone who enjoys developing and supporting a highperforming team while remaining closely connected to complex strategic opportunitiesWe are hiring a Manager Proposal Management to join Fortreas Enterprise C

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Senior Coding Specialist Mexico Candidates must be based in MexicoAre you passionate about medical coding quality and clinical data integrity Were looking for a Senior Coding Specialist based in Mexico to support highquality compliant clinical trial data across global studies.What yo

Senior Coding Specialist Mexico Candidates must be based in MexicoAre you passionate about medical coding quality and clinical data integrity Were looking for a Senior Coding Specialist based in Mexico to support highquality compliant clinical trial data across global studies.What yo

Job Overview:Responsibility for the annual country specific QC plan monitoring and coordinating the implementation and execution of QC plan in the respective country/US region according to the Client Standard Operating Procedures and ICH Guidelines and GCP. Responsibility for the mana

Job Overview:Responsibility for the annual country specific QC plan monitoring and coordinating the implementation and execution of QC plan in the respective country/US region according to the Client Standard Operating Procedures and ICH Guidelines and GCP. Responsibility for the mana

Job Overview:Were seeking a Workday Configuration Developer Manager to assist with design and endtoend solutioning across our Workday PATT portfolioSummary of Responsibilities:Configure andmaintainWorkday Payroll Absence and Time Tracking modules to meet complex business requirements.

Job Overview:Were seeking a Workday Configuration Developer Manager to assist with design and endtoend solutioning across our Workday PATT portfolioSummary of Responsibilities:Configure andmaintainWorkday Payroll Absence and Time Tracking modules to meet complex business requirements.