Fortrea

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

Lead Global Growth Inspire Teams and Shape the Future at FortreaJoin Fortrea as Our Next Executive Director of Business Development!Are you a visionary leader ready to drive innovation and growth in the life sciences industry Fortrea is seeking an exceptional Executive Director of Bus

Lead Global Growth Inspire Teams and Shape the Future at FortreaJoin Fortrea as Our Next Executive Director of Business Development!Are you a visionary leader ready to drive innovation and growth in the life sciences industry Fortrea is seeking an exceptional Executive Director of Bus

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuri

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuri

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

Job Overview:The Clinical Trial Administrator (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 CTA shall reflect their experience and level of contribution which they can mak

Job Overview:The Clinical Trial Administrator (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 CTA shall reflect their experience and level of contribution which they can mak

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

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: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

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

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: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

We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the CRO environment. As a Workd

We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the CRO environment. As a Workd

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

We are currently seeking Sr CRAs with 4 years of monitoring or CRA 2 level candidates (2 years of monitoring) as well as Oncology monitoring experience residing in the North East US. Travel is expected to be regional and about 30% overnight. Job Overview:The Senior CRA 2 is responsibl

We are currently seeking Sr CRAs with 4 years of monitoring or CRA 2 level candidates (2 years of monitoring) as well as Oncology monitoring experience residing in the North East US. Travel is expected to be regional and about 30% overnight. Job Overview:The Senior CRA 2 is responsibl

We are looking for a Senior Centralized Study Associate to join our team in Bulgaria.Summary of Responsibilities:Manage clinical systems and access management.Manage study documents and support eTMF management.Maintain study databases (CTMS IWRS EDC etc.)Support study team in data rev

We are looking for a Senior Centralized Study Associate to join our team in Bulgaria.Summary of Responsibilities:Manage clinical systems and access management.Manage study documents and support eTMF management.Maintain study databases (CTMS IWRS EDC etc.)Support study team in data rev