Fortrea

Fortrea is currently seeking a US remote based Sr Specialist Clinical Data Strategy & Operations (CDSO) FSP to drive and support process development evaluation and implementations projects that are led by the CDSO Process Excellence and Delivery team or co-led with the Global Develop

Fortrea is currently seeking a US remote based Sr Specialist Clinical Data Strategy & Operations (CDSO) FSP to drive and support process development evaluation and implementations projects that are led by the CDSO Process Excellence and Delivery team or co-led with the Global Develop

Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

Job Overview:It is the responsibility of the postholder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. They will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974

Job Overview:It is the responsibility of the postholder to provide all clients both internal and external with the appropriate quality of service in a safe and cost-effective manner. They will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Be responsible for end-to-end report management including planning authoring and managing review approval and submission steps per project scope and r

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

Fortrea is seeking anAssociate Project Finance Associate to join our Project Finance Management team.This entry-level role is ideal for early-career professionalslooking to grow their financial acumen in a global matrixed environment. You will support project financial tracking report

Fortrea is seeking anAssociate Project Finance Associate to join our Project Finance Management team.This entry-level role is ideal for early-career professionalslooking to grow their financial acumen in a global matrixed environment. You will support project financial tracking report

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing in Alberta and Montreal Canada.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for partic

Our FSP team is currently seeking a Sr. CRA 2 with 4 years of monitoring as well as strong Oncology monitoring experience residing in Alberta and Montreal Canada.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for partic

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

Summary of Responsibilities:Develop and review contracts for low to medium complexity projects and see through to execution (including MSAs CDAs ISAs IPAs WSCs budgets if required etc.) up to 50% on MSAs (single unit Client or single unit Fortrea template).Lead negotiations for all a

Summary of Responsibilities:Develop and review contracts for low to medium complexity projects and see through to execution (including MSAs CDAs ISAs IPAs WSCs budgets if required etc.) up to 50% on MSAs (single unit Client or single unit Fortrea template).Lead negotiations for all a

Job Overview:Support site(s) by providing guidance and EHS knowledge to help minimize employee illness and injuries. Assist in ensuring compliance with regulatory requirements and relevant industry standards and help identify and lower EHS-related risks such as fires and environmental

Job Overview:Support site(s) by providing guidance and EHS knowledge to help minimize employee illness and injuries. Assist in ensuring compliance with regulatory requirements and relevant industry standards and help identify and lower EHS-related risks such as fires and environmental

Job Overview:Minimum 23-year experience in a similar job in pharmaceutical companies international CRO or providers of clinical digital servicesReports directly to the FSP Fortrea Line Manager.Receives projects-specific requests and strategic-operational guidance from the Head of Clin

Job Overview:Minimum 23-year experience in a similar job in pharmaceutical companies international CRO or providers of clinical digital servicesReports directly to the FSP Fortrea Line Manager.Receives projects-specific requests and strategic-operational guidance from the Head of Clin

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

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

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:Achieves annual sales plan and sales targets for assigned accou

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:Achieves annual sales plan and sales targets for assigned accou

Fortreas FSP Team is hiring a CRA 1 in Miami or Orlando Florida. Seeking 6 months of recent independent monitoring experience. Oncology required Spanish speaking highly preferred.Job Overview:Site monitoring and site management responsibility for clinical studies according to Company

Fortreas FSP Team is hiring a CRA 1 in Miami or Orlando Florida. Seeking 6 months of recent independent monitoring experience. Oncology required Spanish speaking highly preferred.Job Overview:Site monitoring and site management responsibility for clinical studies according to Company

Fortreas FSP team is hiring a Manager Site Agreements!Home Based in USA and able to work EST hours.Must have 5 years of investigator budget and contract negotiation experience working with CROs and sites globally and experience as a point of escalation. Strong Phase III and oncology e

Fortreas FSP team is hiring a Manager Site Agreements!Home Based in USA and able to work EST hours.Must have 5 years of investigator budget and contract negotiation experience working with CROs and sites globally and experience as a point of escalation. Strong Phase III and oncology e

Job Overview:Performs independent programming activities (using Medidata Rave) on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medida

Job Overview:Performs independent programming activities (using Medidata Rave) on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medida

Job Overview:Leads validation projects as assigned and serve as a validation team member on multiple assignments as designated by the management with support from other team members as needed. Serve as a member of the project team with primary responsibility for all documentation requ

Job Overview:Leads validation projects as assigned and serve as a validation team member on multiple assignments as designated by the management with support from other team members as needed. Serve as a member of the project team with primary responsibility for all documentation requ

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:Minimum 8-year experience in epidemiology pharmacoepidemiology non-interventional studies (prospective studies patient registries retrospective database studies) RWE generation in biopharmaceutical industry or CROs. Reports directly to the FSP Fortrea Line Manager. Receiv

Job Overview:Minimum 8-year experience in epidemiology pharmacoepidemiology non-interventional studies (prospective studies patient registries retrospective database studies) RWE generation in biopharmaceutical industry or CROs. Reports directly to the FSP Fortrea Line Manager. Receiv