Fortrea

***Free parking onsite just steps away from the clinic***Straight Weekend Night Shifts Only: (8 10 or 12 hour shifts available)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

***Free parking onsite just steps away from the clinic***Straight Weekend Night Shifts Only: (8 10 or 12 hour shifts available)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

Summary of Responsibilities:Site management for clinical studies is conducted in accordance with Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and sponsor requirements. This includes verifying that study training records are complete and accurate.S

Summary of Responsibilities:Site management for clinical studies is conducted in accordance with Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and sponsor requirements. This includes verifying that study training records are complete and accurate.S

This individual will leverage advanced analytics and data science techniques to support the Commercial Sales organization through actionable insights predictive modeling and data-driven strategies. The role is critical in enabling evidence-based decision-making optimizing prospecting

This individual will leverage advanced analytics and data science techniques to support the Commercial Sales organization through actionable insights predictive modeling and data-driven strategies. The role is critical in enabling evidence-based decision-making optimizing prospecting

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

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: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

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

We are currently seeking Experienced Oncology CRA 2s to lead and support our Full Service Outsourcing team. CAR-T desired. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgem

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

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

Job Overview:Reporting to the VP Commercial and Enterprise Apps and Quality the Solutions Architect will be responsible for providing architectural leadership and direction for the EPC technology domains of the organization. The Solutions architect will partner across all areas of IT

Job Overview:Reporting to the VP Commercial and Enterprise Apps and Quality the Solutions Architect will be responsible for providing architectural leadership and direction for the EPC technology domains of the organization. The Solutions architect will partner across all areas of IT

Job Overview:Responsible for executing all site purchasing decisions and general maintenance of facility. The position will maintain a vendor database and provide support for all purchasing decisions. The position will also maintain documentation for the maintenance of all facility eq

Job Overview:Responsible for executing all site purchasing decisions and general maintenance of facility. The position will maintain a vendor database and provide support for all purchasing decisions. The position will also maintain documentation for the maintenance of all facility eq

We are currently seeking Experienced Ophthalmology CRA 2s to lead and support our Full Service Outsourcing team. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to pro

We are currently seeking Experienced Ophthalmology CRA 2s to lead and support our Full Service Outsourcing team. Open to major hub locations on the East & West Coast. 60-70% travel 8-10 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to pro

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Achieves annual sales plan and sales targets for assigned accou

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Achieves annual sales plan and sales targets for assigned accou

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 report Adverse Drug Reaction in timelines (according to the regulations and to int

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 report Adverse Drug Reaction in timelines (according to the regulations and to int

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: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

Fortreas FSP team is hiring an Assistant Clinical Quality Control Manager home based in the US. Seeking strong Sr. CRA candidates that are fluent in Japanese or other languages. Job Overview:Responsible for the tracking processing and reporting to functional stakeholders of Quality Co

Fortreas FSP team is hiring an Assistant Clinical Quality Control Manager home based in the US. Seeking strong Sr. CRA candidates that are fluent in Japanese or other languages. Job Overview:Responsible for the tracking processing and reporting to functional stakeholders of Quality Co

Fortreas Clinical Pharmacology Team is hiring a CRA 2 with Phase I experience in Dallas Texas!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 emergency situations based

Fortreas Clinical Pharmacology Team is hiring a CRA 2 with Phase I experience in Dallas Texas!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 emergency situations based

Summary of Responsibilities:Owns all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client r

Summary of Responsibilities:Owns all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client r

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

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