Fortrea

Our FSO team is seeking a Respiratory Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. Job Overview:At times working under the direction of

Our FSO team is seeking a Respiratory Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. Job Overview:At times working under the direction of

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Fortreas FSP team is hiring Budget Builder & Site Contract Specialist!Home Based in USA or Canada. Must have 2 years of budget/contract negotiation experience at CRO level direct site facing experience and experience building global budget templates.As part of a global team you will b

Fortreas FSP team is hiring Budget Builder & Site Contract Specialist!Home Based in USA or Canada. Must have 2 years of budget/contract negotiation experience at CRO level direct site facing experience and experience building global budget templates.As part of a global team you will b

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

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

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 Budget & Contract Specialist you will play a critical role in negotiating and managing budget site agreements confi

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 Budget & Contract Specialist you will play a critical role in negotiating and managing budget site agreements confi

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

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

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

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

Fortrea is recruiting!Our FSP department in Paris is looking fora Senior Clinical Research Associate II (SCRA II).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National o

Fortrea is recruiting!Our FSP department in Paris is looking fora Senior Clinical Research Associate II (SCRA II).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National o

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

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

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

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

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

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

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

*** 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)

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

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