Fortrea

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

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

Have you ever thought that your planning / scheduling skills could save livesAs one of the worlds largest Clinical Research Organizations Fortrea operates four ultramodern Clinical Research Units in the UK and US. Our crown jewel is Drapers Yard in Leedsa brand-new state-of-the-art 65

Have you ever thought that your planning / scheduling skills could save livesAs one of the worlds largest Clinical Research Organizations Fortrea operates four ultramodern Clinical Research Units in the UK and US. Our crown jewel is Drapers Yard in Leedsa brand-new state-of-the-art 65

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

Our FSO team is seeking an Ophthalmology Clinical Project Manager I to join our growing team. This role requires 4 years of global project coordination experience with mandatory experience in ophthalmology. Candidates must be based in the United States. Job Overview:Project Managers o

Our FSO team is seeking an Ophthalmology Clinical Project Manager I to join our growing team. This role requires 4 years of global project coordination experience with mandatory experience in ophthalmology. Candidates must be based in the United States. Job Overview:Project Managers o

Turn Your First Years on the Ward into a New Career PathHave your first 12 years on a hospital ward not turned out the way you expectedAt Fortreas Early Clinical Research Unit in Drapers Yard Leeds you can use that hard-earned experience in a different way helping shape new medical tr

Turn Your First Years on the Ward into a New Career PathHave your first 12 years on a hospital ward not turned out the way you expectedAt Fortreas Early Clinical Research Unit in Drapers Yard Leeds you can use that hard-earned experience in a different way helping shape new medical tr

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 an Clinical Research Coordinator Assistant to interact directly with our healthy volunteer participants while learning to read

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 an Clinical Research Coordinator Assistant to interact directly with our healthy volunteer participants while learning to read