Fortrea

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 Sr. GMP Quality Specialist to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical tri

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 Sr. GMP Quality Specialist to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical tri

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 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

Fortrea is continuously looking for new talents! We are currently searching for Start-Up Specialist for our Sponsor-dedicated department:Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May

Fortrea is continuously looking for new talents! We are currently searching for Start-Up Specialist for our Sponsor-dedicated department:Responsibilities (but not only):Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.May

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

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

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: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 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

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 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

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

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 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

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 ResponsibilitiesManage clinical trial sites in line with Fortrea SOPs ICH G

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 ResponsibilitiesManage clinical trial sites in line with Fortrea SOPs ICH G

Doc Review Specialist I US Joining Fortrea as a Document Review Specialist I today and you will have a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team.The Document Review Specialist I role is responsible for reviewi

Doc Review Specialist I US Joining Fortrea as a Document Review Specialist I today and you will have a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team.The Document Review Specialist I role is responsible for reviewi

Clinical Study ICF Writer US Remote basedFortrea is looking for a confident seasoned Doc Review Senior Specialist who can work independently while collaborating with globally based team members. This individual will provide full and independent review of global project and country re

Clinical Study ICF Writer US Remote basedFortrea is looking for a confident seasoned Doc Review Senior Specialist who can work independently while collaborating with globally based team members. This individual will provide full and independent review of global project and country re

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