Fortrea

We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journeyFORTREA IN LEEDS WHERE MEDICAL BREAKTHROUGHS BEGINAt Fortrea our world-class Clinical Research Unit in Leeds sits at the heart of innovation. Just a short 7-min

We exist to bring new medicines to life. What if your administrative support expertise could help us accelerate that journeyFORTREA IN LEEDS WHERE MEDICAL BREAKTHROUGHS BEGINAt Fortrea our world-class Clinical Research Unit in Leeds sits at the heart of innovation. Just a short 7-min

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

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

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

Job Overview:Responsible for preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices. Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. Assist

Job Overview:Responsible for preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices. Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. Assist

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

Competitive basic salary monthly bonus. Office based Leeds. 25 days holiday ( public holidays) pension healthcare insurance life and accidental death insurance income protection insurance employee discounts and flexible benefits.What if your telephone skills are what we need to make

Competitive basic salary monthly bonus. Office based Leeds. 25 days holiday ( public holidays) pension healthcare insurance life and accidental death insurance income protection insurance employee discounts and flexible benefits.What if your telephone skills are what we need to make

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:Highly organized and detail-oriented Facilities Associate to oversee the reception office management maintenance and procurement needs of our 2 offices located in Sydney and Melbourne Australia. The ideal candidate will be responsible for front of house duties event plann

Job Overview:Highly organized and detail-oriented Facilities Associate to oversee the reception office management maintenance and procurement needs of our 2 offices located in Sydney and Melbourne Australia. The ideal candidate will be responsible for front of house duties event plann

Looking for flexible work where your phone skills can help make new medicines safer for patientsFortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enj

Looking for flexible work where your phone skills can help make new medicines safer for patientsFortreas Clinical Research Unit in Leeds is where life-saving medicines begin their journey.Youll be part of a team that asks one crucial question: will this new medicine be safe If you enj

What if your pharmacy experience helped new medicines take their first step in human clinical trialsFortrea is one of the worlds largest and longestestablished earlyphase clinical research organizations.We operate Phase I Clinical Research Units (CRU) globally including our worldclass

What if your pharmacy experience helped new medicines take their first step in human clinical trialsFortrea is one of the worlds largest and longestestablished earlyphase clinical research organizations.We operate Phase I Clinical Research Units (CRU) globally including our worldclass

Job Overview:Assist with the overall safety system implementation support configuration and migration related activities. Responsible for providing this service to clients either as a support function to the client project pgroups or as stand- alone business. Responsible for providing

Job Overview:Assist with the overall safety system implementation support configuration and migration related activities. Responsible for providing this service to clients either as a support function to the client project pgroups or as stand- alone business. Responsible for providing

This role is for upcoming future opportunities that may arise at 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

This role is for upcoming future opportunities that may arise at 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

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: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

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

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

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

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

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