Fortrea

Job Overview:Our FSO team is seeking an Ophthalmology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3 years of global project management experience with mandatory experience in ophthalmology.Project Managers own the operational strategy

Job Overview:Our FSO team is seeking an Ophthalmology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3 years of global project management experience with mandatory experience in ophthalmology.Project Managers own the operational strategy

Job Overview:Our FSO team is seeking an Oncology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3 years of global project management experience with mandatory experience in oncology.Project Managers own the operational strategy determini

Job Overview:Our FSO team is seeking an Oncology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3 years of global project management experience with mandatory experience in oncology.Project Managers own the operational strategy determini

Job Overview:Our FSO team is seeking a General Medicine Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3 years of global project management experience with mandatory experience in General Medicine.Project Managers own the operational str

Job Overview:Our FSO team is seeking a General Medicine Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3 years of global project management experience with mandatory experience in General Medicine.Project Managers own the operational str

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

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

What if your pharmacy leadership helped new medicines take their first step in human clinical trialsFortrea formerly Covance is one of the worlds largest and longestestablished earlyphase clinical research organizations.We operate Phase I clinical research units (CRU) globally includi

What if your pharmacy leadership helped new medicines take their first step in human clinical trialsFortrea formerly Covance is one of the worlds largest and longestestablished earlyphase clinical research organizations.We operate Phase I clinical research units (CRU) globally includi

At Fortrea your monitoring work directly protects patients and strengthens the quality of the data that moves trials forward. Join our talent community for upcoming CRA opportunities where youll support one sposor and help accelerate lifechanging treatments to the people who need them

At Fortrea your monitoring work directly protects patients and strengthens the quality of the data that moves trials forward. Join our talent community for upcoming CRA opportunities where youll support one sposor and help accelerate lifechanging treatments to the people who need them

Job Overview:Provide enterprise oversight and assurance that quality and compliance systems processes and performance meet applicable laws regulations SOPs protocols and sponsor/CRO requirements. Accountable for portfolio-level quality reliability inspection readiness and risk posture

Job Overview:Provide enterprise oversight and assurance that quality and compliance systems processes and performance meet applicable laws regulations SOPs protocols and sponsor/CRO requirements. Accountable for portfolio-level quality reliability inspection readiness and risk posture

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:Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Committ

Job Overview:Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Committ

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position you will be fully dedicated to a single sponsor. This position is open for full-time candidates.Responsibilities/Provide end-to-end operational oversight for the assigned study(ies) including

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position you will be fully dedicated to a single sponsor. This position is open for full-time candidates.Responsibilities/Provide end-to-end operational oversight for the assigned study(ies) including

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 settings (i.e. unsolicited reports). Manage and process ex

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 settings (i.e. unsolicited reports). Manage and process ex

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and anci

Job Overview:The Clinical and Ancillary Supplies Services (CASS) Specialist II: Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a simple global study. Act as contact with study team during clinical and anci

Job Overview:Senior 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

Job Overview:Senior 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

Job Overview:In the role you will collaborate with key stakeholders across the organization and at times be client facing to achieve client-centric delivery in a matrix organization. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Commit

Job Overview:In the role you will collaborate with key stakeholders across the organization and at times be client facing to achieve client-centric delivery in a matrix organization. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Commit

Job Overview:Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE Oracle Inform CRF Design and Data Capture or imaging activities including proactive prevention strategies. Develop and maintain programs for creation of dat

Job Overview:Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE Oracle Inform CRF Design and Data Capture or imaging activities including proactive prevention strategies. Develop and maintain programs for creation of dat

Job Overview:The Medical Writer supports client engagements and internal requests projects and business development efforts by doing the necessary research data collection analysis and interpretation; development of value messages dossiers reports and other written deliverables modeli

Job Overview:The Medical Writer supports client engagements and internal requests projects and business development efforts by doing the necessary research data collection analysis and interpretation; development of value messages dossiers reports and other written deliverables modeli

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Wor

Job Overview:It is the responsibility of the post holder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Wor

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the succes

Job Overview:The Scientist supports client engagements by contributing to the collection and analysis of primary and secondary data andassistingin the development of client deliverables. This role focuses on executing project-specific tasks applying analytical methods and supporting p

Job Overview:The Scientist supports client engagements by contributing to the collection and analysis of primary and secondary data andassistingin the development of client deliverables. This role focuses on executing project-specific tasks applying analytical methods and supporting p