Fortrea

Job Overview:We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assig

Job Overview:We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assig

Job Overview:We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assig

Job Overview:We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assig

Job Overview:We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assig

Job Overview:We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assig

Fortrea is looking for an experienced clinical operations professional to join our team as Senior Site Navigator with a strong focus on clinical trial startup activities and in-house CRA responsibilities. This role is ideal for someone with solid startup expertise who is ready to take

Fortrea is looking for an experienced clinical operations professional to join our team as Senior Site Navigator with a strong focus on clinical trial startup activities and in-house CRA responsibilities. This role is ideal for someone with solid startup expertise who is ready to take

Provide administrative support to the Japan Site Navigator (SN) team by handling routine operational and document-management tasks. This role will help reduce administrative workload currently performed by SN staff enabling them to focus on study start-up and site management activitie

Provide administrative support to the Japan Site Navigator (SN) team by handling routine operational and document-management tasks. This role will help reduce administrative workload currently performed by SN staff enabling them to focus on study start-up and site management activitie

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

Are you detail-oriented and passionate about supporting clinical research operationsIf so join our team in Bucharest as a Clinical Trial Coordinator where youll play a key role in supporting clinical studies. This is a sponsor-dedicated office-based position (hybrid model) offering me

Are you detail-oriented and passionate about supporting clinical research operationsIf so join our team in Bucharest as a Clinical Trial Coordinator where youll play a key role in supporting clinical studies. This is a sponsor-dedicated office-based position (hybrid model) offering me

Our FSO team is seeking a Respiratory Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. Job Overview:At times working under the direction of

Our FSO team is seeking a Respiratory Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. Job Overview:At times working under the direction of

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Summary of Responsibilities:Draft review negotiate and finalize Clinical Trial Agreements (CTAs) confidentiality agreements amendments and related site contract documentation.Coordinate with sponsors legal teams clinical operations and study teams to facilitate timely contract executi

Fortreas FSP team is hiring Budget Builder & Site Contract Specialist!Home Based in USA or Canada. Must have 2 years of budget/contract negotiation experience at CRO level direct site facing experience and experience building global budget templates.As part of a global team you will b

Fortreas FSP team is hiring Budget Builder & Site Contract Specialist!Home Based in USA or Canada. Must have 2 years of budget/contract negotiation experience at CRO level direct site facing experience and experience building global budget templates.As part of a global team you will b

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead

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 ex

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 ex

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

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

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

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

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

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

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

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

Fortrea is recruiting!Our FSP department in Paris is looking fora Senior Clinical Research Associate II (SCRA II).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National o

Fortrea is recruiting!Our FSP department in Paris is looking fora Senior Clinical Research Associate II (SCRA II).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National o

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a

Job Overview: Assist with the overall Safety system implementation support configuration and Migrationrelated activities. Responsible for providing this service to clients either as a support function to the client projectgroups or as stand- alone business. Responsible for providing a