Fortrea

Job Overview:Responsible for Quality Risk Management activities for combination products by assisting with risk assessments technical documentation compliance reviews and CAPA initiatives. Collaborate with cross-functional teams to ensure product quality regulatory compliance and cont

Job Overview:Responsible for Quality Risk Management activities for combination products by assisting with risk assessments technical documentation compliance reviews and CAPA initiatives. Collaborate with cross-functional teams to ensure product quality regulatory compliance and cont

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

Job Overview:The Director Site Engagement and Partnership Delivery will drive global department strategies that lead to operational effectiveness as it relates to site partner performance. They will lead the global vision and partnership expansion and strategic partner collaborations

Job Overview:The Director Site Engagement and Partnership Delivery will drive global department strategies that lead to operational effectiveness as it relates to site partner performance. They will lead the global vision and partnership expansion and strategic partner collaborations

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

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: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

CRA II Sweden We are currently recruiting a CRA II based in Sweden to support multiple sponsor projects across the Nordic region.As a CRA II you will be responsible for conducting all aspects of site monitoring including site initiation routine monitoring and close-out visits while e

CRA II Sweden We are currently recruiting a CRA II based in Sweden to support multiple sponsor projects across the Nordic region.As a CRA II you will be responsible for conducting all aspects of site monitoring including site initiation routine monitoring and close-out visits while e

Job Overview:Corporate Counsel provides legal support and counseling for Fortrea and their business leaders for matters focusing particularly on vendor and clinical site this role you will work closely with experienced legal and business partners to support contracting risk managemen

Job Overview:Corporate Counsel provides legal support and counseling for Fortrea and their business leaders for matters focusing particularly on vendor and clinical site this role you will work closely with experienced legal and business partners to support contracting risk managemen

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

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the NYC Metro or PHL area.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 to

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in the NYC Metro or PHL area.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 to

*** 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)

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

Join Fortrea and play a key role in advancing clinical research while ensuring the highest standards of patient safety and data quality. This is a client-dedicated Unblinded CRA I role supporting clinical trials where access to treatment assignment information is required.What youll d

Join Fortrea and play a key role in advancing clinical research while ensuring the highest standards of patient safety and data quality. This is a client-dedicated Unblinded CRA I role supporting clinical trials where access to treatment assignment information is required.What youll d

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

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

*** 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)

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

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

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