Fortrea

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

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

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

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

The Executive Director Enterprise Architecture is a senior architecture leadership role accountable for shaping and advancing the enterprise technology blueprint that enables scale resilience modernization and business growth across the organization. This leader guides the Enterprise

The Executive Director Enterprise Architecture is a senior architecture leadership role accountable for shaping and advancing the enterprise technology blueprint that enables scale resilience modernization and business growth across the organization. This leader guides the Enterprise

Main Responsibilities The Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site subject & study level review as applicable) activities and in assisting the execution of several key activities.The Central Monitoring Specialist collaborates with

Main Responsibilities The Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site subject & study level review as applicable) activities and in assisting the execution of several key activities.The Central Monitoring Specialist collaborates with

We are seeking a UKbased Site Start-Up (SSU) Specialist to join our highperforming and collaborative team supporting the delivery of earlyphase clinical trials (Phase I and Phase Ib). This role plays a critical part in enabling timely study startup within the UK working closely with F

We are seeking a UKbased Site Start-Up (SSU) Specialist to join our highperforming and collaborative team supporting the delivery of earlyphase clinical trials (Phase I and Phase Ib). This role plays a critical part in enabling timely study startup within the UK working closely with F

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

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

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

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

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

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

Workflow Manager Pharmacovigilance Operations (Specialist II PSS) US RemoteFortrea is seeking a Workflow Manager Pharmacovigilance Operations (Specialist II PSS) is responsible for supporting and overseeing Clinical Safety and Pharmacovigilance Services (PSS) operations associated wit

Workflow Manager Pharmacovigilance Operations (Specialist II PSS) US RemoteFortrea is seeking a Workflow Manager Pharmacovigilance Operations (Specialist II PSS) is responsible for supporting and overseeing Clinical Safety and Pharmacovigilance Services (PSS) operations associated wit

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

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

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

***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

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