Fortrea

Job Overview:Analyze training needs in collaboration with subject matter experts and relevant stakeholders. Delivers and implements training for employees with learning principles and appropriate standard operating procedures and regulatory guidelines (where applicable). Ensures the i

Job Overview:Analyze training needs in collaboration with subject matter experts and relevant stakeholders. Delivers and implements training for employees with learning principles and appropriate standard operating procedures and regulatory guidelines (where applicable). Ensures the i

*** Please note that this role requires you have experience with taking vitals blood draws and ECGs.***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a OPV (Outpatient Visit)

*** Please note that this role requires you have experience with taking vitals blood draws and ECGs.***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a OPV (Outpatient Visit)

Fortrea is seeking Oncology Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 3 years of experience. Prior monitoring experience required. Remote US or Canada based. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research tria

Fortrea is seeking Oncology Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 3 years of experience. Prior monitoring experience required. Remote US or Canada based. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research tria

Our FSO team is seeking an Oncology Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in oncology. Candidates must be based in the United States. Job Overview:At

Our FSO team is seeking an Oncology Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience with mandatory experience in oncology. Candidates must be based in the United States. Job Overview:At

We are currently seeking Experienced CRAs with Radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team working with various sponsors. 1 year of independent CRO/sponsor monitoring required. Open to major hub locations across the US. 60-70% travel

We are currently seeking Experienced CRAs with Radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team working with various sponsors. 1 year of independent CRO/sponsor monitoring required. Open to major hub locations across the US. 60-70% travel

Job Overview:The Designer liaises with consultancy teams and developers to create design concepts for interactive content (e.g. data display presentation or eLearning) that meet the clients requirements and comply with brand guidelines (where necessary). Develops and sources graphical

Job Overview:The Designer liaises with consultancy teams and developers to create design concepts for interactive content (e.g. data display presentation or eLearning) that meet the clients requirements and comply with brand guidelines (where necessary). Develops and sources graphical

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Sr CRA II assures the impleme

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:The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensuri

Job Overview:The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract ensuri

Job Overview:Responsible for providing coordination and support of projects operated by the Adjudication Services department to ensure smooth delivery and achievement of the objective that all adjudication events are processed and submitted for adjudication within the agreed upon proc

Job Overview:Responsible for providing coordination and support of projects operated by the Adjudication Services department to ensure smooth delivery and achievement of the objective that all adjudication events are processed and submitted for adjudication within the agreed upon proc

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per mo

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per mo

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 HR Business Analyst Special Projects is responsible for supporting and leading strategic HR initiatives projects and process improvements that enhance organizational effectiveness and operational efficiency. This role partners with HR leaders Centers of Excellence and

Job OverviewThe HR Business Analyst Special Projects is responsible for supporting and leading strategic HR initiatives projects and process improvements that enhance organizational effectiveness and operational efficiency. This role partners with HR leaders Centers of Excellence and

Are you passionate about clinical trial budgeting financial strategy and delivering accurate competitive study cost estimatesJoin Fortrea as an Investigator Grants Manager / Clinical Trial Costing Managerand play a critical role in shaping successful clinical research proposals and st

Are you passionate about clinical trial budgeting financial strategy and delivering accurate competitive study cost estimatesJoin Fortrea as an Investigator Grants Manager / Clinical Trial Costing Managerand play a critical role in shaping successful clinical research proposals and st

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the East Coast Midwest & West Coast US!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond t

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the East Coast Midwest & West Coast US!WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond t

Job Overview:Manage Client or Project specific 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) for specified projects. Manage and

Job Overview:Manage Client or Project specific 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) for specified projects. Manage and

Job Overview:The Senior Director Commercial and Marketing Technology Platforms plays a pivotal role in shaping and delivering Fortreas commercial and marketing technology ecosystem. This leader is responsible for the strategy management and continuous evolution of platforms that enabl

Job Overview:The Senior Director Commercial and Marketing Technology Platforms plays a pivotal role in shaping and delivering Fortreas commercial and marketing technology ecosystem. This leader is responsible for the strategy management and continuous evolution of platforms that enabl

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a CRF Specialist to be responsible for transcribing and managing study data ensuring accuracy and collaborating with various st

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a CRF Specialist to be responsible for transcribing and managing study data ensuring accuracy and collaborating with various st

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

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