Fortrea

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 assigned to more junior staff. Assume responsibility for all DM activities (from study star

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 assigned to more junior staff. Assume responsibility for all DM activities (from study star

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 assigned to more junior staff. Assume responsibility for all DM activities (from study star

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 assigned to more junior staff. Assume responsibility for all DM activities (from study star

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 assigned to more junior staff. Assume responsibility for all DM activities (from study star

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 assigned to more junior staff. Assume responsibility for all DM activities (from study star

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Site Budget and Contract Lead to join a sponsordedic

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Site Budget and Contract Lead to join a sponsordedic

Clinical Trial Administrator (CTA)Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of global clinical trials by providing essential operational and administrative support to study teams.Key ResponsibilitiesSupport the coordination and tracking of clinica

Clinical Trial Administrator (CTA)Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of global clinical trials by providing essential operational and administrative support to study teams.Key ResponsibilitiesSupport the coordination and tracking of clinica

This is a dual role of supporting India labour related compliance and being a member of the talent acquisition teamKey Responsibilities:LABOUR GOVERNANCE COMPLIANCE Stay abreast of changes in labour laws statutory regulations labour codes and compliance requirements applicable across

This is a dual role of supporting India labour related compliance and being a member of the talent acquisition teamKey Responsibilities:LABOUR GOVERNANCE COMPLIANCE Stay abreast of changes in labour laws statutory regulations labour codes and compliance requirements applicable across

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Drive Clinical Research Success!AtFortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As aSite Start-Up Specialistyou will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring

Join Our Team and Drive Clinical Research Success!AtFortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As aSite Start-Up Specialistyou will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring

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

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Site Budget and Contract Lead to join a sponsordedic

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Site Budget and Contract Lead to join a sponsordedic

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

Clinical Research Physician Dallas Phase I OnsiteFortrea is hiring a dynamic Clinical Research Physician at our Dallas TX Phase I site onsite full-time and fully immersed in cutting-edge clinical trials. If youre ready to lead with purpose grow your expertise and collaborate with a d

Clinical Research Physician Dallas Phase I OnsiteFortrea is hiring a dynamic Clinical Research Physician at our Dallas TX Phase I site onsite full-time and fully immersed in cutting-edge clinical trials. If youre ready to lead with purpose grow your expertise and collaborate with a d

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

Role objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of creative processes methodologies data and technologies that will ensure ongoing improvements in t

Role objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of creative processes methodologies data and technologies that will ensure ongoing improvements in t

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

The Site Identification & Selection Associate will oversee and ensure the successful delivery of global (end-to-end) site identification and selection (strategy plans activities timelines synthesis of site/investigator insights and presentation to study teams) at a program/study level

The Site Identification & Selection Associate will oversee and ensure the successful delivery of global (end-to-end) site identification and selection (strategy plans activities timelines synthesis of site/investigator insights and presentation to study teams) at a program/study level

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Be the connection between science and solutions. As a Clinical Research Associate you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with

Be the connection between science and solutions. As a Clinical Research Associate you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with

Role objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of creative processes methodologies data and technologies that will ensure ongoing improvements in t

Role objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of creative processes methodologies data and technologies that will ensure ongoing improvements in t