Fortrea

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

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring residing in the Southeast US. 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 situatio

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring residing in the Southeast US. 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 situatio

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expendable

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expendable

Site Navigator ILocation: remoteWe are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to grow their

Site Navigator ILocation: remoteWe are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to grow their

Job Overview:Responsible for handling all public inquiries pertaining to study participation. Schedules screening appointments for qualified participants.Summary of Responsibilities:Receiving and placing calls from and to potential study participants.Enter medical history and demograp

Job Overview:Responsible for handling all public inquiries pertaining to study participation. Schedules screening appointments for qualified participants.Summary of Responsibilities:Receiving and placing calls from and to potential study participants.Enter medical history and demograp

As a Sr Proposal Associate youll play a pivotal role in driving the proposal process for RFIs and RFPs. This role is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating across global teams and business units to deliver high-quality client-focuse

As a Sr Proposal Associate youll play a pivotal role in driving the proposal process for RFIs and RFPs. This role is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating across global teams and business units to deliver high-quality client-focuse

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

The mission of our Project Coordinator Academy is to identify early talent and develop you to become Fortrea s leaders of the future. The PC Academy prepares entry-level Project Coordinators to take on critical client-facing tasks as co-pilots to PMs enabling them to build client trus

The mission of our Project Coordinator Academy is to identify early talent and develop you to become Fortrea s leaders of the future. The PC Academy prepares entry-level Project Coordinators to take on critical client-facing tasks as co-pilots to PMs enabling them to build client trus

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

Job Overview:The Principal Strategy & Planning Specialist supports CPS clinical development strategy and external site partnerships by leveraging site capabilities feasibility data and key performance metrics. It collaborates closely with commercial and operational teams to provide st

Job Overview:The Principal Strategy & Planning Specialist supports CPS clinical development strategy and external site partnerships by leveraging site capabilities feasibility data and key performance metrics. It collaborates closely with commercial and operational teams to provide st

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

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

Job Overview:Location: Warsaw (hybrid role)We are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to

Job Overview:Location: Warsaw (hybrid role)We are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to