Fortrea

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

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 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

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

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

Summary of ResponsibilitiesProvides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit ensuring a robust risk-based and inspection-ready quality management system aligned with global regulatory expect

Summary of ResponsibilitiesProvides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit ensuring a robust risk-based and inspection-ready quality management system aligned with global regulatory expect

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

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator 2 in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.Key ResponsibilitiesAssist with initial

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator 2 in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.Key ResponsibilitiesAssist with initial

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

Senior Medical Director Rheumatology - US Remote BasedRaising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicatedUS remotebasedMedical Directoror Senior Medical Directorwith deep expertise inRheumatologyal

Senior Medical Director Rheumatology - US Remote BasedRaising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicatedUS remotebasedMedical Directoror Senior Medical Directorwith deep expertise inRheumatologyal

Job Overview:The Senior Cybersecurity Analyst (SOC Lead) is pivotal in guiding Fortreas Security Operations Center through expert forensic analysis advanced threat detection and rapid incident response. With a focus on using both proprietary and open-source forensic tools this role is

Job Overview:The Senior Cybersecurity Analyst (SOC Lead) is pivotal in guiding Fortreas Security Operations Center through expert forensic analysis advanced threat detection and rapid incident response. With a focus on using both proprietary and open-source forensic tools this role is

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

Summary of ResponsibilitiesProvides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit ensuring a robust risk-based and inspection-ready quality management system aligned with global regulatory expect

Summary of ResponsibilitiesProvides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit ensuring a robust risk-based and inspection-ready quality management system aligned with global regulatory expect

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator I in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.This role is for upcoming future opportu

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator I in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.This role is for upcoming future opportu

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Associate Country Clinical Quality Manager (ACCQM)Location: London UK (Hybrid 2 days per week in the office)About the roleFortrea is seeking an Associate Country Clinical Quality Manager to join our UK client-dedicated team. This role is particularly well suited to experienced SCRAs

Associate Country Clinical Quality Manager (ACCQM)Location: London UK (Hybrid 2 days per week in the office)About the roleFortrea is seeking an Associate Country Clinical Quality Manager to join our UK client-dedicated team. This role is particularly well suited to experienced SCRAs

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health & Safety at Work

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health & Safety at Work

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