Fortrea

The Product Analyst Intern AI & Pharma IT will support the development of digital healthcare solutions by analyzing user data and evaluating product performance. The role involves collaborating with cross-functional teams to improve AI-powered tools used in clinical trials patient po

The Product Analyst Intern AI & Pharma IT will support the development of digital healthcare solutions by analyzing user data and evaluating product performance. The role involves collaborating with cross-functional teams to improve AI-powered tools used in clinical trials patient po

Full time. Remote in the UK Spain Portugal or Greece.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Principal Medical Writer to lead authoring and development of high complexity cli

Full time. Remote in the UK Spain Portugal or Greece.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Principal Medical Writer to lead authoring and development of high complexity cli

Sponsor-dedicated. Full time. Remote in the UK Greece Spain or Portugal.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and develop

Sponsor-dedicated. Full time. Remote in the UK Greece Spain or Portugal.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and develop

Job Overview:Perform various project management and regulatory affairs activities for Fortrea team including performance reviews human resource issues and assist Senior Management in assigning resources to projects as required. Manage coordinate and oversee the overall Regulatory Ope

Job Overview:Perform various project management and regulatory affairs activities for Fortrea team including performance reviews human resource issues and assist Senior Management in assigning resources to projects as required. Manage coordinate and oversee the overall Regulatory Ope

Job Overview:Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement.Summary of Responsibilities:Accountable for the overall payment management of assigned studies whic

Job Overview:Role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement.Summary of Responsibilities:Accountable for the overall payment management of assigned studies whic

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

Fortrea is seeking a dynamic Senior Director OCIO to shape how technology fuels our business this pivotal role youll partner with senior leaders to set the direction of our enterprise IT strategy oversee a highimpact project portfolio streamline how we invest in technology and ensure

Fortrea is seeking a dynamic Senior Director OCIO to shape how technology fuels our business this pivotal role youll partner with senior leaders to set the direction of our enterprise IT strategy oversee a highimpact project portfolio streamline how we invest in technology and ensure

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 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

The Marketing Senior Manager for the Therapy Area Marketing supports the development and execution of therapyspecific marketing strategies that advance business priorities and customer engagement. This role works closely with scientific clinical and commercial stakeholders to translat

The Marketing Senior Manager for the Therapy Area Marketing supports the development and execution of therapyspecific marketing strategies that advance business priorities and customer engagement. This role works closely with scientific clinical and commercial stakeholders to translat

Summary of Responsibilities:Coordinates and oversees Regulatory Authority Ethics Committee/Institutional Review Board Third Body submissions for all study types across multiple countries globally including EU CTR through CTIS platform.Develops submission strategies timelines and progr

Summary of Responsibilities:Coordinates and oversees Regulatory Authority Ethics Committee/Institutional Review Board Third Body submissions for all study types across multiple countries globally including EU CTR through CTIS platform.Develops submission strategies timelines and progr

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

Love writing. Thrive on deadlines. Interested in clinical researchWere hiring an RFI Associate to support global business development opportunities in a fastpaced CRO environment. Youll help manage RFIs endtoend reviewing requirements pulling inputs from SMEs drafting and QCing conte

Love writing. Thrive on deadlines. Interested in clinical researchWere hiring an RFI Associate to support global business development opportunities in a fastpaced CRO environment. Youll help manage RFIs endtoend reviewing requirements pulling inputs from SMEs drafting and QCing conte

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

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: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: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

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per mo

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per mo

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing on the West Coast (California Arizona Colorado Oregon Washington Nevada Utah Idaho New Mexico Wyoming). WHAT YOU WILL DOYou will utilize your skills knowl

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing on the West Coast (California Arizona Colorado Oregon Washington Nevada Utah Idaho New Mexico Wyoming). WHAT YOU WILL DOYou will utilize your skills knowl

Lead Teams. Elevate Operations. Drive StartUp Excellence.Were looking for an inspiring Clinical Operations Manager to lead a team of 20 professionals across clinical operations ensuring excellence in performance quality compliance and delivery.In addition to core Clinical Operations

Lead Teams. Elevate Operations. Drive StartUp Excellence.Were looking for an inspiring Clinical Operations Manager to lead a team of 20 professionals across clinical operations ensuring excellence in performance quality compliance and delivery.In addition to core Clinical Operations