Fortrea

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

This is a potential opportunity that may arise at Fortrea in the future. By applying you will join our talent community and be considered for upcoming openings that match your skills and experience.Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of glob

This is a potential opportunity that may arise at Fortrea in the future. By applying you will join our talent community and be considered for upcoming openings that match your skills and experience.Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of glob

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 looking for an energetic proactive and highly detail-oriented individual to join our team as an HRSD Specialist I Preboarding. This is a full-time fully remote maternity cover position for approximately 18 months with a preferred start date in November.In this role you will su

We are looking for an energetic proactive and highly detail-oriented individual to join our team as an HRSD Specialist I Preboarding. This is a full-time fully remote maternity cover position for approximately 18 months with a preferred start date in November.In this role you will su

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

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. Seeking candidates in the Dallas Texas area with oncology experience. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to pr

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. Seeking candidates in the Dallas Texas area with oncology experience. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to pr

Job Overview:Responsible for the supervision of assigned direct reports within the Fortrea ANZ Site Navigator team. Responsible for detailed performance review and management of assigned direct reports including Annual Performance Management and Development (PMD) and Individual Develo

Job Overview:Responsible for the supervision of assigned direct reports within the Fortrea ANZ Site Navigator team. Responsible for detailed performance review and management of assigned direct reports including Annual Performance Management and Development (PMD) and Individual Develo