Fortrea

Job DescriptionOur FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest (ILINIAKSMIMNMONDSDWI OH) area.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in

Job DescriptionOur FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest (ILINIAKSMIMNMONDSDWI OH) area.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in

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: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

This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor.Role is based in the Oslo area.Key requirement:Minimum 2 years of clinical monitoring experiencePreferably 1 year experience in oncology studiesSummary of R

This role is for upcoming future opportunities that may arise at Fortrea. It is a full-time position supporting a single sponsor.Role is based in the Oslo area.Key requirement:Minimum 2 years of clinical monitoring experiencePreferably 1 year experience in oncology studiesSummary of R

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 decision-making. This role combines people leadership hands-on analytics project management an

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 decision-making. This role combines people leadership hands-on analytics project management an

Job Overview:Site Navigators II plays 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 th

Job Overview:Site Navigators II plays 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 th

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

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

Join Fortrea as a Senior Clinical Research Associate II within a sponsor-dedicated model where you will work exclusively with a leading global biopharmaceutical this role you will support the delivery of high-quality clinical trials across innovative therapies building strong site re

Join Fortrea as a Senior Clinical Research Associate II within a sponsor-dedicated model where you will work exclusively with a leading global biopharmaceutical this role you will support the delivery of high-quality clinical trials across innovative therapies building strong site re

Job OverviewStep beyond traditional monitoring and take on a highly visible relationship-driven role where you can truly influence clinical trial this unique hybrid role you will lead proactive site engagement build long-term partnerships and drive patient recruitment and retention t

Job OverviewStep beyond traditional monitoring and take on a highly visible relationship-driven role where you can truly influence clinical trial this unique hybrid role you will lead proactive site engagement build long-term partnerships and drive patient recruitment and retention t

Fortrea is expanding its client-dedicated team in Warsaw Poland (hybrid) and is seeking an experienced Clinical Operations Manager (Start-Up Manager) to lead country-level clinical trial start-up and delivery.In this role you will take ownership of country operations and regulatory su

Fortrea is expanding its client-dedicated team in Warsaw Poland (hybrid) and is seeking an experienced Clinical Operations Manager (Start-Up Manager) to lead country-level clinical trial start-up and delivery.In this role you will take ownership of country operations and regulatory su

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

Our FSP team is currently seeking a Unblinded Sr. CRA 1 with 3 years of monitoring! Candidates must resided within the United States. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials an

Our FSP team is currently seeking a Unblinded Sr. CRA 1 with 3 years of monitoring! Candidates must resided within the United States. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials an

Summary of Responsibilities:Lead complex studies such as NDA submissions or complex multi-protocol programs potentially coordinating activities across multiple locations providing statistical oversight and attending relevant project meetings.Perform project management activities for i

Summary of Responsibilities:Lead complex studies such as NDA submissions or complex multi-protocol programs potentially coordinating activities across multiple locations providing statistical oversight and attending relevant project meetings.Perform project management activities for i

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

Job Overview:The Associate supports client engagements and internal project team requests and policy projects by developing research plans; conducting research; collecting data and policy information; judging the relevance and applicability of data collected or policies identified; an

Job Overview:The Associate supports client engagements and internal project team requests and policy projects by developing research plans; conducting research; collecting data and policy information; judging the relevance and applicability of data collected or policies identified; an

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

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: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

Job Overview:Site Navigators II plays 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 th

Job Overview:Site Navigators II plays 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 th