Fortrea

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in Northern California. 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 emerg

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5 years of monitoring residing in Northern California. 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 emerg

Job Overview:The Executive Director Biotech Portfolio Lead (BPL) is an enterprise commercial leader accountable for the strategic direction commercial performance and delivery excellence of Fortreas most critical biotech client portfolios. Serving as executive sponsor for a regional p

Job Overview:The Executive Director Biotech Portfolio Lead (BPL) is an enterprise commercial leader accountable for the strategic direction commercial performance and delivery excellence of Fortreas most critical biotech client portfolios. Serving as executive sponsor for a regional p

Job Overview:Directs territory sales strategy and execution collaborating with senior leadership to shape account plans optimize territory performance and drive revenue growth. Leads develops and coaches Business Development Directors while fostering strong client relationships identi

Job Overview:Directs territory sales strategy and execution collaborating with senior leadership to shape account plans optimize territory performance and drive revenue growth. Leads develops and coaches Business Development Directors while fostering strong client relationships identi

Job Overview:Responsible for general maintenance and any required archival of documents produced by the CPS Project Management (PM) Team. Organizing gathering scanning and filing of all applicable documents into appropriate electronic and/or paper copy locations including the Trial Ma

Job Overview:Responsible for general maintenance and any required archival of documents produced by the CPS Project Management (PM) Team. Organizing gathering scanning and filing of all applicable documents into appropriate electronic and/or paper copy locations including the Trial Ma

Summary of Responsibilities:To complete Other duties/activities as assigned by study management team but not limited to:Manage clinical systems and access management.Maintain study databases (CTMS IWRS EDC etc.)Support study team in e-TMF management activities.Support study team in da

Summary of Responsibilities:To complete Other duties/activities as assigned by study management team but not limited to:Manage clinical systems and access management.Maintain study databases (CTMS IWRS EDC etc.)Support study team in e-TMF management activities.Support study team in da

Fortrea is seeking an Country & Site Feasibility Lead to join our FSP team! We are seeking experienced candidates with 4 years of site feasibility experience. Remote US based. Job Overview:The Global Feasibility Lead will play an integral role in operational strategy and planning in

Fortrea is seeking an Country & Site Feasibility Lead to join our FSP team! We are seeking experienced candidates with 4 years of site feasibility experience. Remote US based. Job Overview:The Global Feasibility Lead will play an integral role in operational strategy and planning in

Fortrea is looking for an experienced clinical operations professional to join our team as Site Navigator II (remote) 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

Fortrea is looking for an experienced clinical operations professional to join our team as Site Navigator II (remote) 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

Job Overview:Manages the document classification under Smart Inbox and ARC review (as applicable) as well as document deletion.Summary of Responsibilities:Maintains an understanding of applicable regulatory requirements.Managing electronic Trial Master Files (eTMF) (Trial Country and

Job Overview:Manages the document classification under Smart Inbox and ARC review (as applicable) as well as document deletion.Summary of Responsibilities:Maintains an understanding of applicable regulatory requirements.Managing electronic Trial Master Files (eTMF) (Trial Country and

Fortrea is looking for a Sr Clinical Data Analyst (24 years experience) to join our medical device teamAs a Sr Clinical Data Analyst at Fortrea you will play a key role in ensuring the quality integrity and timeliness of clinical trial data across assigned studies. Working alongside a

Fortrea is looking for a Sr Clinical Data Analyst (24 years experience) to join our medical device teamAs a Sr Clinical Data Analyst at Fortrea you will play a key role in ensuring the quality integrity and timeliness of clinical trial data across assigned studies. Working alongside a

Job Overview:The Executive Director Biotech Portfolio Lead (BPL) is an enterprise commercial leader accountable for the strategic direction commercial performance and delivery excellence of Fortreas most critical biotech client portfolios. Serving as executive sponsor for a regional p

Job Overview:The Executive Director Biotech Portfolio Lead (BPL) is an enterprise commercial leader accountable for the strategic direction commercial performance and delivery excellence of Fortreas most critical biotech client portfolios. Serving as executive sponsor for a regional p

Summary of Responsibilities:The statements below are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities skills and duties.Responsible for all aspects of study site monitoring including routine monitoring and closeou

Summary of Responsibilities:The statements below are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities skills and duties.Responsible for all aspects of study site monitoring including routine monitoring and closeou

Come expand and grow your potential leadership and skills at Fortrea as an (onsite) Physician Assistant (PA) based in our Phase I Dallas TX location supporting clinical trials. The Physician Assistant reports to onsite Medical Director and one of the major functions of the role is com

Come expand and grow your potential leadership and skills at Fortrea as an (onsite) Physician Assistant (PA) based in our Phase I Dallas TX location supporting clinical trials. The Physician Assistant reports to onsite Medical Director and one of the major functions of the role is com

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:The Director Workday Lead is a people leader responsible for guiding the strategic direction governance and operational excellence of the Workday platform across Finance and related enterprise functions. This role oversees a team of Workday specialists and serves as the t

Job Overview:The Director Workday Lead is a people leader responsible for guiding the strategic direction governance and operational excellence of the Workday platform across Finance and related enterprise functions. This role oversees a team of Workday specialists and serves as the t

At Fortrea we are passionate about advancing clinical research and improving patients lives worldwide. We are currently looking for a Site StartUp Clinical Trial Assistant to join our team in a clientdedicated model supporting global clinical trials from setup through activation.This

At Fortrea we are passionate about advancing clinical research and improving patients lives worldwide. We are currently looking for a Site StartUp Clinical Trial Assistant to join our team in a clientdedicated model supporting global clinical trials from setup through activation.This

The Associate II Patient Safety Solutions will manage adverse event reporting and ensure compliance with regulatory timelines.Key Responsibilities:Process and review adverse event reports from clinical trials and post-marketing sources.Enter safety data write patient narratives and co

The Associate II Patient Safety Solutions will manage adverse event reporting and ensure compliance with regulatory timelines.Key Responsibilities:Process and review adverse event reports from clinical trials and post-marketing sources.Enter safety data write patient narratives and co

Work in a CRO That Truly Makes a Difference.AtFortrea our Senior CRAs work across adiverse and challenging environment that reflects where medicine is going not where its been.Your role: Lead and manage sites across varied and complex indications Build trusted relationships with inves

Work in a CRO That Truly Makes a Difference.AtFortrea our Senior CRAs work across adiverse and challenging environment that reflects where medicine is going not where its been.Your role: Lead and manage sites across varied and complex indications Build trusted relationships with inves

What if your clinical operations expertise helped new medicines take their first step in human clinical trialsFortrea is one of the largest and longestestablished earlystage clinical research organizations in the world. We operate four Phase I clinical research units globally includin

What if your clinical operations expertise helped new medicines take their first step in human clinical trialsFortrea is one of the largest and longestestablished earlystage clinical research organizations in the world. We operate four Phase I clinical research units globally includin

What if you were the person clinical research teams relied on when project plans move into live clinic activityFortrea is one of the largest and longestestablished earlystage clinical research organizations in the world. We operate four Phase I clinical research units globally includi

What if you were the person clinical research teams relied on when project plans move into live clinic activityFortrea is one of the largest and longestestablished earlystage clinical research organizations in the world. We operate four Phase I clinical research units globally includi

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