Fortrea

Are you looking to grow your career in clinical researchFortrea is hiring experienced CRAs (minimum of 2 years of independent monitoring experience) on different levels of seniority to join our client-dedicated team. This role is remote offering an exciting opportunity to work on div

Are you looking to grow your career in clinical researchFortrea is hiring experienced CRAs (minimum of 2 years of independent monitoring experience) on different levels of seniority to join our client-dedicated team. This role is remote offering an exciting opportunity to work on div

Job Overview:The Learning Solutions Specialist plays a key role in designing developing and managing learningcontent. This position combines LMS administration with instructional design and content development.The role ensures that learning materials are engaging effective and accessi

Job Overview:The Learning Solutions Specialist plays a key role in designing developing and managing learningcontent. This position combines LMS administration with instructional design and content development.The role ensures that learning materials are engaging effective and accessi

Job Overview:The Salesforce Product Analyst will assist in the development within the Salesforce domain products IT solutions and define the vision strategy and priorities at Fortrea. The Product Analyst gathers and prioritize requirements communicates with stakeholders and make decis

Job Overview:The Salesforce Product Analyst will assist in the development within the Salesforce domain products IT solutions and define the vision strategy and priorities at Fortrea. The Product Analyst gathers and prioritize requirements communicates with stakeholders and make decis

Join Fortrea as a Startup Specialist in a sponsor-dedicated role supporting clinical research for one of our key this position you will drive site activation and regulatory submissions ensuring compliance and timely delivery for global studies.This is a full-time remote role based i

Join Fortrea as a Startup Specialist in a sponsor-dedicated role supporting clinical research for one of our key this position you will drive site activation and regulatory submissions ensuring compliance and timely delivery for global studies.This is a full-time remote role based i

Job Overview:As the Manager of Global Sourcing you will play a crucial role in developing managing and executing category strategies that support Fortreas strategic imperatives and mission. This may include Clinical Services and/or Clinical Technologies (e.g. EDC eCOA) along with Corp

Job Overview:As the Manager of Global Sourcing you will play a crucial role in developing managing and executing category strategies that support Fortreas strategic imperatives and mission. This may include Clinical Services and/or Clinical Technologies (e.g. EDC eCOA) along with Corp

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 preparing grants forecasts for studies through the communications with study teams to understand budget and assumptions. This includes ad hoc requests or reports associated with forecasting and accrual related activities.Summary of Responsibilities:Work wi

Job Overview:Responsible for preparing grants forecasts for studies through the communications with study teams to understand budget and assumptions. This includes ad hoc requests or reports associated with forecasting and accrual related activities.Summary of Responsibilities:Work wi

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 you know when the role officially opens so we can reconfirm your interest

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 you know when the role officially opens so we can reconfirm your interest

Job Overview:As the Manager of Global Sourcing you will play a crucial role in developing managing and executing category strategies that support Fortreas strategic imperatives and mission. This may include Clinical Services and/or Clinical Technologies (e.g. EDC eCOA) along with Corp

Job Overview:As the Manager of Global Sourcing you will play a crucial role in developing managing and executing category strategies that support Fortreas strategic imperatives and mission. This may include Clinical Services and/or Clinical Technologies (e.g. EDC eCOA) along with Corp

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and reporting Adverse Drug Reaction in timelines (according to the regulations and to

Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and reporting Adverse Drug Reaction in timelines (according to the regulations and to

Join Fortrea as a Startup Specialist in a sponsor-dedicated role supporting clinical research for one of our key this position you will drive site activation and regulatory submissions ensuring compliance and timely delivery for global studies.This is a full-time remote role availab

Join Fortrea as a Startup Specialist in a sponsor-dedicated role supporting clinical research for one of our key this position you will drive site activation and regulatory submissions ensuring compliance and timely delivery for global studies.This is a full-time remote role availab

Are you passionate about clinical research and regulatory excellence Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials ensuring compliance quality and timely delivery of study

Are you passionate about clinical research and regulatory excellence Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials ensuring compliance quality and timely delivery of study

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:Responsible for assisting with 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

Job Overview:Responsible for assisting with 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

Job Overview:The Global Feasibility Lead 2 will play an integral role in operational strategy and planning in the preaward space through participation in strategy development conversations robust primary and secondary data collection and analysis and development of feasibility and sit

Job Overview:The Global Feasibility Lead 2 will play an integral role in operational strategy and planning in the preaward space through participation in strategy development conversations robust primary and secondary data collection and analysis and development of feasibility and sit

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

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 you know when the role officially opens so we can reconfirm your interest

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 you know when the role officially opens so we can reconfirm your interest

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

We are looking to bring an experienced Centralized Study Specialist to our team in Bulgaria.Responsibilities will include:Review initial/amended Country/Site ICFs in compliance with Sponsor requirements local regulatory requirements and Good Clinical Practice (GCP) guidelinesReview an

We are looking to bring an experienced Centralized Study Specialist to our team in Bulgaria.Responsibilities will include:Review initial/amended Country/Site ICFs in compliance with Sponsor requirements local regulatory requirements and Good Clinical Practice (GCP) guidelinesReview an

Shape the Future of Data at FortreaAre you a visionary leader in data architecture and integration Fortrea is seeking a Chief Data Officer to drive the strategy and execution of services that will deliver the future state for Fortreas global data platforms.The role will require the de

Shape the Future of Data at FortreaAre you a visionary leader in data architecture and integration Fortrea is seeking a Chief Data Officer to drive the strategy and execution of services that will deliver the future state for Fortreas global data platforms.The role will require the de