Fortrea

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

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 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

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

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

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

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

Job Overview:Document Review Specialist I is responsible for reviewing Investigator Packages Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP FDA and other regional guidance. Document Review Specialist I is responsible for

Job Overview:Document Review Specialist I is responsible for reviewing Investigator Packages Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP FDA and other regional guidance. Document Review Specialist I is responsible for

We are seeking a highly skilled Workday Configuration Lead with deep expertise in Procure-to-Pay (P2P) modules. This senior-level individual contributor role will be responsible for designing building testing and deploying Workday solutions that enable efficient procurement and paymen

We are seeking a highly skilled Workday Configuration Lead with deep expertise in Procure-to-Pay (P2P) modules. This senior-level individual contributor role will be responsible for designing building testing and deploying Workday solutions that enable efficient procurement and paymen

What if your ability to organize complex clinical trials is what helps new medicines reach patients fasterFortrea Clinical Pharmacology Services (CPS) supports the earliest and most critical phases of clinical development. Our teams work across project management clinical operations d

What if your ability to organize complex clinical trials is what helps new medicines reach patients fasterFortrea Clinical Pharmacology Services (CPS) supports the earliest and most critical phases of clinical development. Our teams work across project management clinical operations d

We are seeking a talented and motivated Inside Sales team member that thrives in a sales cycle environment. This member of the team will play a fundamental role in achieving our ambitious revenue growth objectives while collaborating with other Business Development team members.Essent

We are seeking a talented and motivated Inside Sales team member that thrives in a sales cycle environment. This member of the team will play a fundamental role in achieving our ambitious revenue growth objectives while collaborating with other Business Development team members.Essent

Job Overview:As the Manager of Global Sourcing you will play a crucial role in developing managing and executing category strategies that support Fortreas strategic imperatives and mission. You will position the Global Procurement Services organization as a trusted strategic partner a

Job Overview:As the Manager of Global Sourcing you will play a crucial role in developing managing and executing category strategies that support Fortreas strategic imperatives and mission. You will position the Global Procurement Services organization as a trusted strategic partner a

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

Job Overview:The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face continuous learning environment Project Coordinators (PC) are the right-hand support to the Project Lea

Job Overview:The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face continuous learning environment Project Coordinators (PC) are the right-hand support to the Project Lea

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

Fortrea is a leading global contract research organization (CRO) focused on delivering clinical development solutions that accelerate the delivery of therapies to patients worldwide. With deep therapeutic expertise advanced analytics and a global footprint Fortrea partners with pharma

Fortrea is a leading global contract research organization (CRO) focused on delivering clinical development solutions that accelerate the delivery of therapies to patients worldwide. With deep therapeutic expertise advanced analytics and a global footprint Fortrea partners with pharma

Job Overview:Document Review Specialist I is responsible for reviewing Investigator Packages Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP FDA and other regional guidance. Document Review Specialist I is responsible for

Job Overview:Document Review Specialist I is responsible for reviewing Investigator Packages Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP FDA and other regional guidance. Document Review Specialist I is responsible for