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

Job Overview:Assist with the overall Safety trackers / applications / tools implementation support configuration and migration related activities. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. R

Job Overview:Assist with the overall Safety trackers / applications / tools implementation support configuration and migration related activities. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. R

Job DescriptionFortreas FSP team is hiring experienced Sr. Project Managers! Seeking current Sr. PMs with recent experience working for a Sponsor directly or within a FSP model. Oncology experience required. Home Based in the US. Job Overview:At times working under the direction of a

Job DescriptionFortreas FSP team is hiring experienced Sr. Project Managers! Seeking current Sr. PMs with recent experience working for a Sponsor directly or within a FSP model. Oncology experience required. Home Based in the US. Job Overview:At times working under the direction of a

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

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 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 Paramedic III to interact directly with our healthy volunteer participants while learning to read clinical research protocols a

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 Paramedic III to interact directly with our healthy volunteer participants while learning to read clinical research protocols a

Summary of Responsibilities:Investigator Payments:Review EDC Contract and process payments in payment system.Work with PA to generate cover letter or Proforma invoice and payment batch generation in payment system..Perform Invoice QCCoordinate with CTL PM for payment batch approvals.P

Summary of Responsibilities:Investigator Payments:Review EDC Contract and process payments in payment system.Work with PA to generate cover letter or Proforma invoice and payment batch generation in payment system..Perform Invoice QCCoordinate with CTL PM for payment batch approvals.P

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 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

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

We are seeking a motivated Junior Developer Intern to join our pharmaceutical IT team focusing on automating business processes using modern platforms. Youll gain hands-on experience designing and deploying automation solutions that support clinical regulatory and enterprise workflows

We are seeking a motivated Junior Developer Intern to join our pharmaceutical IT team focusing on automating business processes using modern platforms. Youll gain hands-on experience designing and deploying automation solutions that support clinical regulatory and enterprise workflows

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

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:TheCentralized Study Specialist IIis a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to theCentralized Study Specialist IIshall reflect their experience and level of contribution which the

Job Overview:TheCentralized Study Specialist IIis a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to theCentralized Study Specialist IIshall reflect their experience and level of contribution which the

Our FSP Team is hiring SSU Specialists! Remote in the US!Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third b

Our FSP Team is hiring SSU Specialists! Remote in the US!Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third b

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

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide