Fortrea

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

A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha

A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha

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

Providing full support to the Flexible Solutions group to facilitate client delivery by e.g. Support in tracking of compliance KPIs/metrics root causes and mitigations Support in tracking information to support delivery leads in client oversight. Regular updates to reporting tools to

Providing full support to the Flexible Solutions group to facilitate client delivery by e.g. Support in tracking of compliance KPIs/metrics root causes and mitigations Support in tracking information to support delivery leads in client oversight. Regular updates to reporting tools to

Job Title:Centralized study spec I Clinical InvoicingBusiness Title / Posting Title:Centralized study spec IRole Overview:The Business Operations Associate will play a critical role in managing clinical invoicing processes ensuring accuracy compliance and timely execution. This positi

Job Title:Centralized study spec I Clinical InvoicingBusiness Title / Posting Title:Centralized study spec IRole Overview:The Business Operations Associate will play a critical role in managing clinical invoicing processes ensuring accuracy compliance and timely execution. This positi

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Locat

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Locat

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

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

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

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

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

*** Multiple night shifts available as follows******Free parking onsite just steps away from the clinic***Straight Night Shift / Weekdays Only: (12 Hour) 6 PM 6 AMStraight Night Shift / Weekdays Only: (8 Hour) 11 PM 7 AMStraight Night Shift / Weekends Only: (12 Hour) 6 PM 6 AMAs on

*** Multiple night shifts available as follows******Free parking onsite just steps away from the clinic***Straight Night Shift / Weekdays Only: (12 Hour) 6 PM 6 AMStraight Night Shift / Weekdays Only: (8 Hour) 11 PM 7 AMStraight Night Shift / Weekends Only: (12 Hour) 6 PM 6 AMAs on

Summary of Responsibilities:Site management for clinical studies is conducted in accordance with Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and sponsor requirements. This includes verifying that study training records are complete and accurate.S

Summary of Responsibilities:Site management for clinical studies is conducted in accordance with Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and sponsor requirements. This includes verifying that study training records are complete and accurate.S

This individual will leverage advanced analytics and data science techniques to support the Commercial Sales organization through actionable insights predictive modeling and data-driven strategies. The role is critical in enabling evidence-based decision-making optimizing prospecting

This individual will leverage advanced analytics and data science techniques to support the Commercial Sales organization through actionable insights predictive modeling and data-driven strategies. The role is critical in enabling evidence-based decision-making optimizing prospecting

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

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:Responsible for executing all site purchasing decisions and general maintenance of research facility. The position will maintain a vendor database and provide support for all purchasing decisions. The position will also maintain documentation for the maintenance of all fa

Job Overview:Responsible for executing all site purchasing decisions and general maintenance of research facility. The position will maintain a vendor database and provide support for all purchasing decisions. The position will also maintain documentation for the maintenance of all fa

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

Job Overview:Reporting to the VP Commercial and Enterprise Apps and Quality the Solutions Architect will be responsible for providing architectural leadership and direction for the EPC technology domains of the organization. The Solutions architect will partner across all areas of IT

Job Overview:Reporting to the VP Commercial and Enterprise Apps and Quality the Solutions Architect will be responsible for providing architectural leadership and direction for the EPC technology domains of the organization. The Solutions architect will partner across all areas of IT

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