Fortrea

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

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 seeking anAssociate Project Finance Associate to join our Project Finance Management team.This entry-level role is ideal for early-career professionalslooking to grow their financial acumen in a global matrixed environment. You will support project financial tracking report

Fortrea is seeking anAssociate Project Finance Associate to join our Project Finance Management team.This entry-level role is ideal for early-career professionalslooking to grow their financial acumen in a global matrixed environment. You will support project financial tracking report

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

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

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp

Job Overview:Performs independent programming activities (using Medidata Rave) on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medida

Job Overview:Performs independent programming activities (using Medidata Rave) on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medida

Job Overview:Leads validation projects as assigned and serve as a validation team member on multiple assignments as designated by the management with support from other team members as needed. Serve as a member of the project team with primary responsibility for all documentation requ

Job Overview:Leads validation projects as assigned and serve as a validation team member on multiple assignments as designated by the management with support from other team members as needed. Serve as a member of the project team with primary responsibility for all documentation requ

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:Minimum 8-year experience in epidemiology pharmacoepidemiology non-interventional studies (prospective studies patient registries retrospective database studies) RWE generation in biopharmaceutical industry or CROs. Reports directly to the FSP Fortrea Line Manager. Receiv

Job Overview:Minimum 8-year experience in epidemiology pharmacoepidemiology non-interventional studies (prospective studies patient registries retrospective database studies) RWE generation in biopharmaceutical industry or CROs. Reports directly to the FSP Fortrea Line Manager. Receiv

Senior Clinical Data Manager FSP / oncology experienceThe Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management

Senior Clinical Data Manager FSP / oncology experienceThe Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management

Schedule: Full-time Monday-Friday 7am-3pm EST.*** Must be an experienced nurse and skilled in phlebotomy and vitals.***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 Clinic

Schedule: Full-time Monday-Friday 7am-3pm EST.*** Must be an experienced nurse and skilled in phlebotomy and vitals.***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 Clinic

Fortreas FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development.The TMF Management team is responsible for the completeness and accuracy of the Trial Master File (TMF) for all sponsored studies. The TMF Lead II is the Subj

Fortreas FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development.The TMF Management team is responsible for the completeness and accuracy of the Trial Master File (TMF) for all sponsored studies. The TMF Lead II is the Subj

Job Overview:The Director of Cybersecurity Risk Management is responsible for building and maintaining Fortreas cybersecurity risk management function. This leader will oversee IT and third-party cybersecurity risk management - collaborating with peers and leaders across IT global sup

Job Overview:The Director of Cybersecurity Risk Management is responsible for building and maintaining Fortreas cybersecurity risk management function. This leader will oversee IT and third-party cybersecurity risk management - collaborating with peers and leaders across IT global sup

Job Overview:The Senior Director IT Finance isa strategic leadership role responsible for managing and optimizing the entire financial systems landscape and ensuring alignment with overall business objectives and regulatory requirements. This role manages the product backlog for Finan

Job Overview:The Senior Director IT Finance isa strategic leadership role responsible for managing and optimizing the entire financial systems landscape and ensuring alignment with overall business objectives and regulatory requirements. This role manages the product backlog for Finan

Job Overview:Manages ARC review and is responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs.Summary of Responsibilities:Position

Job Overview:Manages ARC review and is responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs.Summary of Responsibilities:Position

Come expand and grow your potential leadership and skills at Fortrea as an (onsite) Physician Assistant (PA) based in our Phase I Madison Wisconsin location supporting clinical trials. The Physician Assistant reports to onsite Medical Director and one of the major functions of the rol

Come expand and grow your potential leadership and skills at Fortrea as an (onsite) Physician Assistant (PA) based in our Phase I Madison Wisconsin location supporting clinical trials. The Physician Assistant reports to onsite Medical Director and one of the major functions of the rol

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 Screening Technician to interact directly with our healthy volunteer participants while learning to read clinical research p

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 Screening Technician to interact directly with our healthy volunteer participants while learning to read clinical research p

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 3 years of monitoring experience to join our FSP team! Experience in Cardiology Device or Electrophysiology is required for this role. This role will include some nationwide travel during start u

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 3 years of monitoring experience to join our FSP team! Experience in Cardiology Device or Electrophysiology is required for this role. This role will include some nationwide travel during start u

Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing qualityinteraction with other departments

Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing qualityinteraction with other departments

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica