Fortrea

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

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

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

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

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

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:Calling Clinical Data Managers / Database designers with strong experience in protocol interpretaion and edit checks specification keen to be trained in programming!Performs programming activities (using Medidata Rave or Veeva) on multiple projects concurrently with less

Job Overview:Calling Clinical Data Managers / Database designers with strong experience in protocol interpretaion and edit checks specification keen to be trained in programming!Performs programming activities (using Medidata Rave or Veeva) on multiple projects concurrently with less

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

Job Overview:Manages the document classification under sponsor system and Fortrea system.Summary of Responsibilities:Maintains an understanding of applicable regulatory requirements.Managing electronic Trial Master Files (eTMF) (Trial Country and Site artifacts) for clinical studies i

Job Overview:Manages the document classification under sponsor system and Fortrea system.Summary of Responsibilities:Maintains an understanding of applicable regulatory requirements.Managing electronic Trial Master Files (eTMF) (Trial Country and Site artifacts) for clinical studies i

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

Associate Director PSS Remote based CanadaWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pa

Associate Director PSS Remote based CanadaWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pa

Do you have a passion for scientific writing and clinical research Then join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials.Fortrea Clinical Pharmacology Services (CPS) supports the earlie

Do you have a passion for scientific writing and clinical research Then join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials.Fortrea Clinical Pharmacology Services (CPS) supports the earlie

Come join Fortrea today as a part time Nurse Practitioner with our Phase I site based in Daytona Beach Florida. The NP - Nurse Practitioner provides clinical expertise and serves as a key knowledge resource for the clinical aspects of trials conducted within Clinical Pharmacology. Thi

Come join Fortrea today as a part time Nurse Practitioner with our Phase I site based in Daytona Beach Florida. The NP - Nurse Practitioner provides clinical expertise and serves as a key knowledge resource for the clinical aspects of trials conducted within Clinical Pharmacology. Thi

Job Overview:It is the responsibility of the postholder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. They will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974

Job Overview:It is the responsibility of the postholder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. They will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974