Fortrea

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

We are seeking a detail-oriented and customer-focused individual to join our team as a Part-time Front Desk this role you will be the first point of contact forguests sponsor auditors and employee visitors ensuring a professional and welcoming experience. You will manage front desk o

We are seeking a detail-oriented and customer-focused individual to join our team as a Part-time Front Desk this role you will be the first point of contact forguests sponsor auditors and employee visitors ensuring a professional and welcoming experience. You will manage front desk o

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigne

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

Join Our Team and Drive Clinical Research Success!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 ensuri

Join Our Team and Drive Clinical Research Success!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 ensuri

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: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

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

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

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

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