Fortrea

We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact this is your chance!Key Responsibilities: In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and regulatory requirementsBuild strong relat

We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact this is your chance!Key Responsibilities: In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and regulatory requirementsBuild strong relat

Job Overview:We are seeking a detail-oriented and proactive Pharmacovigilance Associate II to support Clinical Trial and Post-Approval Case Processing Activities primarily case follow-up activities. The primary responsibility of this role is to collect and process safety data through

Job Overview:We are seeking a detail-oriented and proactive Pharmacovigilance Associate II to support Clinical Trial and Post-Approval Case Processing Activities primarily case follow-up activities. The primary responsibility of this role is to collect and process safety data through

Fortrea is currently seeking a remote based Specialist I (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical knowledge as well as an understanding of the US Healthcare system.This is a full-time home-

Fortrea is currently seeking a remote based Specialist I (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical knowledge as well as an understanding of the US Healthcare system.This is a full-time home-

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

Senior Analyst Real World Evidence (RWE) (Remote): This is a permanent remote opportunity that can be worked from anywhere in U.SWe are seeking a Senior Analyst Real World Evidence (RWE) (US Remote) to provide programming and analysis support for Real World Evidence projects for Fortr

Senior Analyst Real World Evidence (RWE) (Remote): This is a permanent remote opportunity that can be worked from anywhere in U.SWe are seeking a Senior Analyst Real World Evidence (RWE) (US Remote) to provide programming and analysis support for Real World Evidence projects for Fortr

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. This is an excellent opportunity to start

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator in Germany youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites. This is an excellent opportunity to start

Job Overview: The Payroll Coordinator will provide full functional payroll support for the allocated APAC payrolls although primarily home country ensuring they are processed accurately and on-time.They will ensure processing payments and reporting deadlines are met in a timely and ac

Job Overview: The Payroll Coordinator will provide full functional payroll support for the allocated APAC payrolls although primarily home country ensuring they are processed accurately and on-time.They will ensure processing payments and reporting deadlines are met in a timely and ac

Fortrea is looking for an experienced Contract and Budget Lead to support our key client in EMEARole objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of c

Fortrea is looking for an experienced Contract and Budget Lead to support our key client in EMEARole objectivesManage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.Support the development of c

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: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

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

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: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