Fortrea

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

The Costing Manager is a position that sits within the Costing Department as part of the ECS group. The role is primarily charged with supporting the Costing Directors in the delivery of clinical study costings and will predominantly liaise with the Costing Directors on a daily basis.

The Costing Manager is a position that sits within the Costing Department as part of the ECS group. The role is primarily charged with supporting the Costing Directors in the delivery of clinical study costings and will predominantly liaise with the Costing Directors on a daily basis.

Job Overview:The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy such as: Collaborate within a matrix environment communicat

Job Overview:The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy such as: Collaborate within a matrix environment communicat

Change Manager Clinical Data Management / TransformationThe Change Manager role is a great opportunity to work within our FSP team supporting Clinical Data Management activities through a growing portfolio of transformation initiatives. You will play a key role in delivering practica

Change Manager Clinical Data Management / TransformationThe Change Manager role is a great opportunity to work within our FSP team supporting Clinical Data Management activities through a growing portfolio of transformation initiatives. You will play a key role in delivering practica

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:Responsible for the preparation and review of aggregate safety risk management and signal detection documents. Perform report management activities and lead client communication for the assigned reports. Assist other medical writers in their safety deliverables act as a c

Job Overview:Responsible for the preparation and review of aggregate safety risk management and signal detection documents. Perform report management activities and lead client communication for the assigned reports. Assist other medical writers in their safety deliverables act as a c

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

The Workflow Manager Pharmacovigilance Operations is responsible for overseeing optimizing and ensuring the efficient execution of end-to-end case processing and safety workflows. He/she will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974 t

The Workflow Manager Pharmacovigilance Operations is responsible for overseeing optimizing and ensuring the efficient execution of end-to-end case processing and safety workflows. He/she will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974 t

Fortreas FSP team is seeking experienced Sr. CRAs based in Canada with complex cardiacexperience within the past 5 yearspreferably in electrophysiology and / or devices.Must have 3 years of monitoring experience. This role will include some nationwide travel during start up. Job Overv

Fortreas FSP team is seeking experienced Sr. CRAs based in Canada with complex cardiacexperience within the past 5 yearspreferably in electrophysiology and / or devices.Must have 3 years of monitoring experience. This role will include some nationwide travel during start up. Job Overv

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the postmarketing period; and may manage a team.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the postmarketing period; and may manage a team.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case

Fortreas FSP team is seeking experienced West Coast based Sr. CRAs with complex cardiacexperience within the past 5 yearspreferably in electrophysiology and / or devices.Must have 3 years of monitoring experience. This role will include some nationwide travel during start up. Job Over

Fortreas FSP team is seeking experienced West Coast based Sr. CRAs with complex cardiacexperience within the past 5 yearspreferably in electrophysiology and / or devices.Must have 3 years of monitoring experience. This role will include some nationwide travel during start up. Job Over

***Phlebotomy experience required***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 Phlebotomist (On-Call) to interact directly with our healthy volunteer participants while

***Phlebotomy experience required***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 Phlebotomist (On-Call) to interact directly with our healthy volunteer participants while

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enjoy working in a fast-paced environment speaking with people and contributing to meaningful resea

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enjoy working in a fast-paced environment speaking with people and contributing to meaningful resea

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enjoy working in a fast-paced environment speaking with people and contributing to meaningful resea

Fortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enjoy working in a fast-paced environment speaking with people and contributing to meaningful resea

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing in the Toronto Canada area. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participa

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing in the Toronto Canada area. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participa

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

The Solutions Consultant Digital Health and Innovation Senior Director (FIT) is a senior customer-facing commercial leader responsible for driving revenue growth by accelerating market adoption of Fortrea Intelligent Technology (FIT) solutions across FSO FSP and SaaS clinical trial de

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating coverage.We are currently seeking a Screening Receptionist to support the day-to-day administration of medical scr

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating coverage.We are currently seeking a Screening Receptionist to support the day-to-day administration of medical scr

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and reporting Adverse Drug Reaction in timelines (according to the regulations and to

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and reporting Adverse Drug Reaction in timelines (according to the regulations and to

Here in Fortrea Bulgaria we are looking for an experienced CRA to join our multisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed

Here in Fortrea Bulgaria we are looking for an experienced CRA to join our multisponsor team.Responsibilities:Conduct site monitoring visits (initiation routine close-out) in line with SOPs ICH-GCP and study requirementsEnsure patient safety and protocol compliance including informed

Job Overview:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development.Summary of Responsibilities:Contribute to architectural vision for Fortreas data architecture data

Job Overview:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development.Summary of Responsibilities:Contribute to architectural vision for Fortreas data architecture data