Fortrea

Job Overview:The Medical Contact Center Sr. Specialist will be responsible for responding to medical information queries product quality complaints and any general queries that may be received via the Medical Contact Center.Summary of Responsibilities:Receive information record and re

Job Overview:The Medical Contact Center Sr. Specialist will be responsible for responding to medical information queries product quality complaints and any general queries that may be received via the Medical Contact Center.Summary of Responsibilities:Receive information record and re

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially t

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially t

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

Under the guidance of the Regional Director Clinical Quality Management (RCQM) the CCQM oversees all CQM activities in the respective country/cluster.The role requires the ability to properly implement local/global processes/procedures to identify opportunities for process improvement

Under the guidance of the Regional Director Clinical Quality Management (RCQM) the CCQM oversees all CQM activities in the respective country/cluster.The role requires the ability to properly implement local/global processes/procedures to identify opportunities for process improvement

As a Proposal Manager I within Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating ac

As a Proposal Manager I within Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating ac

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

Job Overview:The Clinical Trial Coordinator (CTC) 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 CTC shall reflect their experience and level of contribution which they can make

Job Overview:The Clinical Trial Coordinator (CTC) 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 CTC shall reflect their experience and level of contribution which they can make

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

Are you looking to grow your career in clinical research Fortrea is hiring experienced CRAs to join our client-dedicated team. We have opportunities based in Ireland offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company

Are you looking to grow your career in clinical research Fortrea is hiring experienced CRAs to join our client-dedicated team. We have opportunities based in Ireland offering an exciting chance to work on diverse studies while ensuring compliance with regulatory guidelines and company

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

We are currently seeking Experienced Oncology CRAs residing in the Central & Midwest US to join our FSP team! Various openings include regional travel as well as nationwide travel options. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high

We are currently seeking Experienced Oncology CRAs residing in the Central & Midwest US to join our FSP team! Various openings include regional travel as well as nationwide travel options. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high

We are currently seeking a Clinical Quality Operations Manager!This is a full-time hybrid role based within Canada. This individual will need to be located in Canada Fluent in French and English and willing to go into the Montreal/Kirkland office twice a week.If you join us you will w

We are currently seeking a Clinical Quality Operations Manager!This is a full-time hybrid role based within Canada. This individual will need to be located in Canada Fluent in French and English and willing to go into the Montreal/Kirkland office twice a week.If you join us you will w

Fortrea is hiring a dynamic Clinical Research Physician at our Dallas TX Phase I site onsite full-time and fully immersed in cutting-edge clinical trials. If youre ready to lead with purpose grow your expertise and collaborate with a dynamic team this role could be your next big move

Fortrea is hiring a dynamic Clinical Research Physician at our Dallas TX Phase I site onsite full-time and fully immersed in cutting-edge clinical trials. If youre ready to lead with purpose grow your expertise and collaborate with a dynamic team this role could be your next big move

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

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

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:Works with Global Sales and Client Services Business Unit Presi

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:Works with Global Sales and Client Services Business Unit Presi

Job DescriptionThe Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially

Job DescriptionThe Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially

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: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

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were seeking a highly motivated and detail-oriented Pharmacy Technician who thrives in a fast-paced regulated environment and is eager to grow within th

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were seeking a highly motivated and detail-oriented Pharmacy Technician who thrives in a fast-paced regulated environment and is eager to grow within th

We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact this is your chance!Key Responsibilities: In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and regulatory requirementsBuild strong relat

We are seeking a Sponsor-Dedicated CRA with solid monitoring experience. If you are eager to make an impact this is your chance!Key Responsibilities: In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and regulatory requirementsBuild strong relat