Fortrea

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

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

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

*** Multiple night shifts available as follows******Free parking onsite just steps away from the clinic***Straight Night Shift / Weekdays Only: (12 Hour) 6 PM 6 AMStraight Night Shift / Weekdays Only: (8 Hour) 11 PM 7 AMStraight Night Shift / Weekends Only: (12 Hour) 6 PM 6 AMAs on

*** Multiple night shifts available as follows******Free parking onsite just steps away from the clinic***Straight Night Shift / Weekdays Only: (12 Hour) 6 PM 6 AMStraight Night Shift / Weekdays Only: (8 Hour) 11 PM 7 AMStraight Night Shift / Weekends Only: (12 Hour) 6 PM 6 AMAs on

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

A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha

A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha

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 Title:Centralized study spec I Clinical InvoicingBusiness Title / Posting Title:Centralized study spec IRole Overview:The Business Operations Associate will play a critical role in managing clinical invoicing processes ensuring accuracy compliance and timely execution. This positi

Job Title:Centralized study spec I Clinical InvoicingBusiness Title / Posting Title:Centralized study spec IRole Overview:The Business Operations Associate will play a critical role in managing clinical invoicing processes ensuring accuracy compliance and timely execution. This positi

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Locat

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Locat

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 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