Fortrea

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

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory submissions are completed efficientl

At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory submissions are completed efficientl

Job Overview:Service Delivery People Services Center contact receives inquiries on service central and provide employee support. Performs workload fulfillment for Service Delivery activities (e.g. HR invoices offer administration and employee services) and enters information into admi

Job Overview:Service Delivery People Services Center contact receives inquiries on service central and provide employee support. Performs workload fulfillment for Service Delivery activities (e.g. HR invoices offer administration and employee services) and enters information into admi

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Perform data management activities such as clinical data review query generation / resolution and reconciliation activities to support the Lead Data Reviewer/LDM with the delivery of clinical data according to client quality project timelines and productivity targets.Summ

Job Overview:Perform data management activities such as clinical data review query generation / resolution and reconciliation activities to support the Lead Data Reviewer/LDM with the delivery of clinical data according to client quality project timelines and productivity targets.Summ

Job Overview:Perform data management activities such as clinical data review query generation / resolution and reconciliation activities to support the Lead Data Reviewer/LDM with the delivery of clinical data according to client quality project timelines and productivity targets.Summ

Job Overview:Perform data management activities such as clinical data review query generation / resolution and reconciliation activities to support the Lead Data Reviewer/LDM with the delivery of clinical data according to client quality project timelines and productivity targets.Summ

Job DescriptionOur FSP team is currently seeking In-house CRA IIs to join our FSP team! Prior CRO experience preferred. Remote based US. Job Overview:The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical Project Team responsible for the execution

Job DescriptionOur FSP team is currently seeking In-house CRA IIs to join our FSP team! Prior CRO experience preferred. Remote based US. Job Overview:The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical Project Team responsible for the execution

Fortreas Monitoring Excellence Academy is hiring!! We are seeking strong Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2 years of current experience. Must have 2 years of Oncology CAR T or Ophthalmology experience as a CRC or research to various Cen

Fortreas Monitoring Excellence Academy is hiring!! We are seeking strong Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2 years of current experience. Must have 2 years of Oncology CAR T or Ophthalmology experience as a CRC or research to various Cen

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 Administrative Assistant I to interact directly with our healthy volunteer participants while learning to read clinical rese

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 Administrative Assistant I to interact directly with our healthy volunteer participants while learning to read clinical rese

Our FSP team is currently seeking a CRA 2 in Central Region with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in cli

Our FSP team is currently seeking a CRA 2 in Central Region with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in cli

Our FSP team is currently seeking a CRA 2 in Ohio Pennsylvania or Virginia with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for part

Our FSP team is currently seeking a CRA 2 in Ohio Pennsylvania or Virginia with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for part

Our FSP team is currently seeking Oncology CRA 2s on the East Coast! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and re

Our FSP team is currently seeking Oncology CRA 2s on the East Coast! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and re

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 an Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical r

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 an Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical r

Job Overview:The Executive Director HR and Workday Platform Technology is the primary technology platform leader for Human Resources and Facilities and the enterprise platform owner for Workday. This role is accountable for the strategic leadership operational stability governance pro

Job Overview:The Executive Director HR and Workday Platform Technology is the primary technology platform leader for Human Resources and Facilities and the enterprise platform owner for Workday. This role is accountable for the strategic leadership operational stability governance pro

The Executive Director HR and Workday Platform Technology is the primary technology platform leader for Human Resources and Facilities and the enterprise platform owner for Workday. This role is accountable for the strategic leadership operational stability governance product roadmap

The Executive Director HR and Workday Platform Technology is the primary technology platform leader for Human Resources and Facilities and the enterprise platform owner for Workday. This role is accountable for the strategic leadership operational stability governance product roadmap

Job Overview:The Clinical Trial Investigator Grant Forecasting delivers the defined outcomes associated with maintaining and improving forecasts for investigator grants and related site-level clinical trial payments across the global clinical development portfolio. The role partners c

Job Overview:The Clinical Trial Investigator Grant Forecasting delivers the defined outcomes associated with maintaining and improving forecasts for investigator grants and related site-level clinical trial payments across the global clinical development portfolio. The role partners c

Job Overview:The Aggregate Report Specialist is responsible for supporting core pharmacovigilance deliverables including scheduled and ad hoc aggregate reports while ensuring high-quality timely execution of assigned activities. The role involves collaboration with cross-functional st

Job Overview:The Aggregate Report Specialist is responsible for supporting core pharmacovigilance deliverables including scheduled and ad hoc aggregate reports while ensuring high-quality timely execution of assigned activities. The role involves collaboration with cross-functional st