Fortrea

Job Overview:The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client in compliance with ICH GCP and country regulat

Job Overview:The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client in compliance with ICH GCP and country regulat

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

Clinical Team Lead Phase IAre you passionate clinical research professional ready to lead the charge in groundbreaking trials Join Fortrea as a Phase I Clinical Team Lead (CTL) and drive clinical project excellence!About the RoleAs a Phase I Clinical Team Lead youll own the clinical d

Clinical Team Lead Phase IAre you passionate clinical research professional ready to lead the charge in groundbreaking trials Join Fortrea as a Phase I Clinical Team Lead (CTL) and drive clinical project excellence!About the RoleAs a Phase I Clinical Team Lead youll own the clinical d

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

Summary of Responsibilities:Follow all applicable departmental Standard Operating Procedures and Work Instructions.Complete day-to-day tasks ensuring quality and productivity.Execute high quality timely monitoring and reporting plan(s) including specialized monitoring requests for app

Summary of Responsibilities:Follow all applicable departmental Standard Operating Procedures and Work Instructions.Complete day-to-day tasks ensuring quality and productivity.Execute high quality timely monitoring and reporting plan(s) including specialized monitoring requests for app

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let

Job Overview:As the Senior Manager of Global Sourcing you will lead strategic sourcing initiatives and manage the end-to-end Source to Contract process for assigned categories. This may include Clinical Technologies (e.g. EDC eCOA) along with Corporate/Enterprise Technologies and/or C

Job Overview:As the Senior Manager of Global Sourcing you will lead strategic sourcing initiatives and manage the end-to-end Source to Contract process for assigned categories. This may include Clinical Technologies (e.g. EDC eCOA) along with Corporate/Enterprise Technologies and/or C

Overview:This role supports financial activities within the site readiness and regulatory operations team with a focus on contract management and budget oversight for clinical projects.Key Responsibilities:Act as the primary contact for financial matters related to site activation and

Overview:This role supports financial activities within the site readiness and regulatory operations team with a focus on contract management and budget oversight for clinical projects.Key Responsibilities:Act as the primary contact for financial matters related to site activation and

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

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

Job Overview:The Medical Contact Center Sr. Specialist will be responsible for responding to medical information queries product quality complaints and any general queries that may be received via the Medical Contact Center.Summary of Responsibilities:Receive information record and re

Job Overview:The Medical Contact Center Sr. Specialist will be responsible for responding to medical information queries product quality complaints and any general queries that may be received via the Medical Contact Center.Summary of Responsibilities:Receive information record and re

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially t

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially t

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

Under the guidance of the Regional Director Clinical Quality Management (RCQM) the CCQM oversees all CQM activities in the respective country/cluster.The role requires the ability to properly implement local/global processes/procedures to identify opportunities for process improvement

Under the guidance of the Regional Director Clinical Quality Management (RCQM) the CCQM oversees all CQM activities in the respective country/cluster.The role requires the ability to properly implement local/global processes/procedures to identify opportunities for process improvement

As a Proposal Manager I within Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating ac

As a Proposal Manager I within Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating ac

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:The Clinical Trial Coordinator (CTC) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTC shall reflect their experience and level of contribution which they can make

Job Overview:The Clinical Trial Coordinator (CTC) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTC shall reflect their experience and level of contribution which they can make

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

Are you looking to grow your career in clinical research Fortrea is hiring experienced CRAs to join our client-dedicated team. We have opportunities based in Ireland offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company

Are you looking to grow your career in clinical research Fortrea is hiring experienced CRAs to join our client-dedicated team. We have opportunities based in Ireland offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company

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