Fortrea

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 Director Clinical Operations to interact directly with our healthy volunteer participants while learning to read clinical res

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 Director Clinical Operations to interact directly with our healthy volunteer participants while learning to read clinical res

Job Overview:The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA II shall reflect their experience and level of contributi

Job Overview:The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA II shall reflect their experience and level of contributi

Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments

Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments

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

Job Overview:The Director Global Strategic Sourcing is responsible for leading the strategy design and development of a world-class strategic sourcing and category management function for one or more categories or segments within Fortreas global sourcing scope. This leader must have t

Job Overview:The Director Global Strategic Sourcing is responsible for leading the strategy design and development of a world-class strategic sourcing and category management function for one or more categories or segments within Fortreas global sourcing scope. This leader must have t

Fortrea is looking for CRA I to join FSO department.You Responsibilities (but not only):Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with v

Fortrea is looking for CRA I to join FSO department.You Responsibilities (but not only):Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with v

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:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Maintains an understanding of applicable r

Job Overview:Responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Maintains an understanding of applicable r

We are currently seeking an experienced Global Start Up Project Manager with 3 years of SUPM experience to join our team! Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and

We are currently seeking an experienced Global Start Up Project Manager with 3 years of SUPM experience to join our team! Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and

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

Summary of Responsibilities:Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc. (Language: French)Receive information record and report Adverse Drug Reaction in timelines (according to the regula

Summary of Responsibilities:Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc. (Language: French)Receive information record and report Adverse Drug Reaction in timelines (according to the regula

Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversight to ensure all activities are conducted to the highest possible quality and in accordance with

Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversight to ensure all activities are conducted to the highest possible quality and in accordance with

Job Overview:As a Workday Extend Developer at Fortrea you will be responsible for designing developing and implementing custom applications and integrations within the Workday platform. You will work closely with cross-functional teams to understand business requirements develop solut

Job Overview:As a Workday Extend Developer at Fortrea you will be responsible for designing developing and implementing custom applications and integrations within the Workday platform. You will work closely with cross-functional teams to understand business requirements develop solut

The QA Lead Manager is responsible for overseeing Quality Issue Management ensuring GCP compliance and providing expert QA support across clinical development teams. This role partners closely with crossfunctional stakeholders to investigate quality issues drive effective CAPA develop

The QA Lead Manager is responsible for overseeing Quality Issue Management ensuring GCP compliance and providing expert QA support across clinical development teams. This role partners closely with crossfunctional stakeholders to investigate quality issues drive effective CAPA develop

We are looking for a clinical operations professional to join our team as a Site Navigator II with a significant Start-Up experience. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.Summary of Responsibilities:Act

We are looking for a clinical operations professional to join our team as a Site Navigator II with a significant Start-Up experience. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.Summary of Responsibilities:Act

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:The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience and level of contribution whi

Job Overview:The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience and level of contribution whi

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: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