Fortrea

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

Job OverviewThe Associate HR Partner Clinical Research Units (CRUs) CPS is a clinic-aligned HR specialist role that provides hands-on onsite HR support to CPS Clinical Research Units. This role partners closely with Clinic Senior Directors site leadership and HR Business Partners to s

Job OverviewThe Associate HR Partner Clinical Research Units (CRUs) CPS is a clinic-aligned HR specialist role that provides hands-on onsite HR support to CPS Clinical Research Units. This role partners closely with Clinic Senior Directors site leadership and HR Business Partners to s

Fortrea is currently recruiting a CRA II to join our multisponsor team in Poland on a permanent full-time contract.This is a unique opportunity for a CRA based in Poland to support clinical trial monitoring in the UK and Ireland. The role may involve regular travel abroad to conduct o

Fortrea is currently recruiting a CRA II to join our multisponsor team in Poland on a permanent full-time contract.This is a unique opportunity for a CRA based in Poland to support clinical trial monitoring in the UK and Ireland. The role may involve regular travel abroad to conduct o

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

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:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development. The role of the informatics team is to lead breakthrough innovations that will unlock the power o

Job Overview:Informatics at Fortrea is a high profile high impact team that focuses on creating innovative data-driven solutions to improve the speed cost and quality of drug development. The role of the informatics team is to lead breakthrough innovations that will unlock the power o

Job Overview:Responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs.Summary of Responsibilities:Position provides process control

Job Overview:Responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs.Summary of Responsibilities:Position provides process control

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:Site Navigators play 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 this r

Job Overview:Site Navigators play 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 this r

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expendable

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expendable

Key Responsibilities:Strategic Operational Leadership:Serve as a leader within theCommercial Account Management team contributing to the development and execution of the groups strategic roadmap.Lead the strategic planning and execution of global biotechstrategyinitiatives as applicab

Key Responsibilities:Strategic Operational Leadership:Serve as a leader within theCommercial Account Management team contributing to the development and execution of the groups strategic roadmap.Lead the strategic planning and execution of global biotechstrategyinitiatives as applicab

Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned.Responsible for all asp

Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned.Responsible for all asp

Job Overview:We areseekinga highly skilled Workday Configuration Analyst with deepexpertisein Procure-to-Pay (P2P) modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that enable efficient procurement

Job Overview:We areseekinga highly skilled Workday Configuration Analyst with deepexpertisein Procure-to-Pay (P2P) modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that enable efficient procurement

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

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:Responsible to follow GMP and safety practice

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:Responsible to follow GMP and safety practice

Are you detail-oriented and passionate about supporting clinical research operations Join our team in Munich as a Project Coordinator (Clinical or Budget&Finance focus) where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor

Are you detail-oriented and passionate about supporting clinical research operations Join our team in Munich as a Project Coordinator (Clinical or Budget&Finance focus) where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor

Job Overview:We are looking for an experienced Workday Configuration Analyst with deepexpertisein Payroll Absence and Time Tracking modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that support our

Job Overview:We are looking for an experienced Workday Configuration Analyst with deepexpertisein Payroll Absence and Time Tracking modules. This senior-level individual contributor role willbe responsible fordesigning building testing and deploying Workday solutions that support our

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

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

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