Fortrea

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

Job Overview:The Executive Director Business Development is a strategic business partner who leads a team of Business Development Directors at all levels to develop and expand new business opportunities while growing and maintaining existing accounts. The role steers overall growth in

Job Overview:The Executive Director Business Development is a strategic business partner who leads a team of Business Development Directors at all levels to develop and expand new business opportunities while growing and maintaining existing accounts. The role steers overall growth in

Our CPS team is currently seeking a Study Start Up Specialist with 2 years of start-up experience residing with the U.S. Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investiga

Our CPS team is currently seeking a Study Start Up Specialist with 2 years of start-up experience residing with the U.S. Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investiga

As an experienced Senior RWE Biostatistician within our Consulting business you will play a pivotal role in delivering complex Real-World Evidence (RWE) non-interventional and low-interventional research studies for leading global pharmaceutical and biotechnology companies. Working as

As an experienced Senior RWE Biostatistician within our Consulting business you will play a pivotal role in delivering complex Real-World Evidence (RWE) non-interventional and low-interventional research studies for leading global pharmaceutical and biotechnology companies. Working as

Position OverviewThe Accounting Senior Associate will play a key role in supporting the monthly and quarterly consolidated close process ensuring timely accurate and well-controlled financial reporting deliverables. This role requires a highly analytical accounting professional with a

Position OverviewThe Accounting Senior Associate will play a key role in supporting the monthly and quarterly consolidated close process ensuring timely accurate and well-controlled financial reporting deliverables. This role requires a highly analytical accounting professional with 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 a Patient Meal Server to interact directly with our healthy volunteer participants while learning to read clinical research pro

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 Patient Meal Server to interact directly with our healthy volunteer participants while learning to read clinical research pro

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in Texas or Mid-West (Kansas Missouri Nebraska Iowa Colorado). WHAT YOU WILL DOYou will utilize your skills knowledge and clinical

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in Texas or Mid-West (Kansas Missouri Nebraska Iowa Colorado). WHAT YOU WILL DOYou will utilize your skills knowledge and clinical

Job Overview:Assist with the overall Safety system 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. Responsible for providing

Job Overview:Assist with the overall Safety system 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. Responsible for providing

Our FSP team is currently seeking a CRA 2 in West 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 clinic

Our FSP team is currently seeking a CRA 2 in West 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 clinic

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in California. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for

Our Phase I team is currently seeking a Clinical Research Associate with 1 years of experience. Ideal candidates would have phase I experience and reside in California. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for

Job Overview:Provide foundational operational support to the supplier qualification lifecycle ensuring accurate documentation and compliance with procedures.Summary of Responsibilities:Support defined steps of the supplier qualification and requalification processes.Accurately collect

Job Overview:Provide foundational operational support to the supplier qualification lifecycle ensuring accurate documentation and compliance with procedures.Summary of Responsibilities:Support defined steps of the supplier qualification and requalification processes.Accurately collect

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest area.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 respond to emergency

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the Midwest area.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 respond to emergency

Our FSP team is currently seeking an Ophthalmology Sr. CRA 2 with 5 years of monitoring residing in the Midwest area. Oncology experience may be considered as well. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for par

Our FSP team is currently seeking an Ophthalmology Sr. CRA 2 with 5 years of monitoring residing in the Midwest area. Oncology experience may be considered as well. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for par

Job Overview:The Director/Senior Director Participant Recruitment & Engagementis responsible forthe strategic leadership development and execution of participant recruitment engagement and retention initiatives that support clinical trial enrollmentobjectivesacross Clinical Pharmacolo

Job Overview:The Director/Senior Director Participant Recruitment & Engagementis responsible forthe strategic leadership development and execution of participant recruitment engagement and retention initiatives that support clinical trial enrollmentobjectivesacross Clinical Pharmacolo

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

Our Phase I team is currently seeking a Senior Clinical Research Associate with 3 years of experience. Ideal candidates would have phase I experience and reside in the U.S.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care

Our Phase I team is currently seeking a Senior Clinical Research Associate with 3 years of experience. Ideal candidates would have phase I experience and reside in the U.S.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care

Job Overview:The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site subject and study level review as applicable) activities and in assisting the execution of several key activities. The Central Monitoring Specialist collaborates with the st

Job Overview:The Central Monitoring Specialist is responsible for the execution of key Central monitoring (Site subject and study level review as applicable) activities and in assisting the execution of several key activities. The Central Monitoring Specialist collaborates with the st

Fortrea is recruiting!Fortrea in Paris is looking fora Senior Clinical Research Associate I (SCRA I) to be Sponsor-Dedicated.Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) -

Fortrea is recruiting!Fortrea in Paris is looking fora Senior Clinical Research Associate I (SCRA I) to be Sponsor-Dedicated.Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) -

Job Overview:Assist with the overall Safety system 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. Responsible for providing

Job Overview:Assist with the overall Safety system 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. Responsible for providing

Job Overview:The Senior Business Development Director Early Phase leads portfolio-level growth by developing and executing strategies that expand market presence and maximize account value focused on a broader portfolio of high-priority accounts. The role engages senior client and int

Job Overview:The Senior Business Development Director Early Phase leads portfolio-level growth by developing and executing strategies that expand market presence and maximize account value focused on a broader portfolio of high-priority accounts. The role engages senior client and int