Fortrea

Senior Technical Designer Medidata RAVE certifiedJoin our growing team and discover your extraordinary potential by working as a Senior Technical Designer within our division working with some of our most important sponsors. The position offers a strong support network flexible worki

Senior Technical Designer Medidata RAVE certifiedJoin our growing team and discover your extraordinary potential by working as a Senior Technical Designer within our division working with some of our most important sponsors. The position offers a strong support network flexible worki

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuri

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuri

Clinical Data Manager - Early Phase full remote or hybridDo you have experience leading data management activities across early phase studies Are you looking for a new challenge in an environment where youwill be closely supported by your Manager peers and Senior Leaders in your team

Clinical Data Manager - Early Phase full remote or hybridDo you have experience leading data management activities across early phase studies Are you looking for a new challenge in an environment where youwill be closely supported by your Manager peers and Senior Leaders in your team

The Specialist Fulfilment Associate will lead adverse event followup activities for Participating Affiliate Pharma ICSRs with limited supervision ensuring regulatory compliance and audit readiness. This role supports operational excellence through accurate execution proactive issue re

The Specialist Fulfilment Associate will lead adverse event followup activities for Participating Affiliate Pharma ICSRs with limited supervision ensuring regulatory compliance and audit readiness. This role supports operational excellence through accurate execution proactive issue re

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were seeking a highly motivated and detail-oriented Pharmacy Technician who thrives in a fast-paced regulated environment and is eager to grow within th

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were seeking a highly motivated and detail-oriented Pharmacy Technician who thrives in a fast-paced regulated environment and is eager to grow within th

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated US remote based Medical Director or Senior Medical Director with deep expertise in Oncology along with background in innovative therapies includi

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated US remote based Medical Director or Senior Medical Director with deep expertise in Oncology along with background in innovative therapies includi

At Fortrea we are redefining the clinical research landscape through innovation collaboration and a commitment to improving health worldwide. Join a global team where your expertise drives meaningful impact and your career growth is supported every step of the way.About the RoleAs a S

At Fortrea we are redefining the clinical research landscape through innovation collaboration and a commitment to improving health worldwide. Join a global team where your expertise drives meaningful impact and your career growth is supported every step of the way.About the RoleAs a S

Have you ever wanted to see a clinical trial happen in real timeThis is not monitoring from a distance. At Fortrea Clinical Pharmacology Services in Leeds CRAs are on site in the flow of the study when it matters most.You see dosing days. You walk the clinic floor. You review data as

Have you ever wanted to see a clinical trial happen in real timeThis is not monitoring from a distance. At Fortrea Clinical Pharmacology Services in Leeds CRAs are on site in the flow of the study when it matters most.You see dosing days. You walk the clinic floor. You review data as

Senior Clinical Data Manager fully home-basedJoining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from

Senior Clinical Data Manager fully home-basedJoining Fortreas Clinical Data Management sponsor dedicated team will offer a rewarding career a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from

Were looking for a Site Start-Up Clinical Trial Assistant to support key site activation activities and help bring groundbreaking treatments to patients faster. Are you ready to play a vital role in the success of clinical trialsKey Responsibilities Support SSU team in executing clini

Were looking for a Site Start-Up Clinical Trial Assistant to support key site activation activities and help bring groundbreaking treatments to patients faster. Are you ready to play a vital role in the success of clinical trialsKey Responsibilities Support SSU team in executing clini

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated US remote based Medical Director or Senior Medical Director with deep expertise in Oncology along with background in innovative therapies includi

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated US remote based Medical Director or Senior Medical Director with deep expertise in Oncology along with background in innovative therapies includi

Job Overview:The Executive Compensation Senior Manager is responsible for supporting the design administration analysis and governance of executive compensation programs including base salary shortterm incentives and longterm incentives. The role partners with internal specialists and

Job Overview:The Executive Compensation Senior Manager is responsible for supporting the design administration analysis and governance of executive compensation programs including base salary shortterm incentives and longterm incentives. The role partners with internal specialists and

Job Overview:The Senior Clinical Site Director is responsible for the management administration and organization of local site operations for a Clinical Pharmacology unit may take on responsibility for multiple sites. Responsible for the overall performance of the site(s) meeting defi

Job Overview:The Senior Clinical Site Director is responsible for the management administration and organization of local site operations for a Clinical Pharmacology unit may take on responsibility for multiple sites. Responsible for the overall performance of the site(s) meeting defi

We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device & Diagnostics team! Open to major hub locations across the US. 60-70% travel 7-9 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high sta

We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device & Diagnostics team! Open to major hub locations across the US. 60-70% travel 7-9 DOS per month. WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high sta

Fortrea is looking for a Clinical Data Scientist - R Programmer to join our team in Poland in a fully remote setup.In this role you will support Centralized Monitoring by configuring and maintaining systems setting up new studies and developing standard and bespoke monitoring function

Fortrea is looking for a Clinical Data Scientist - R Programmer to join our team in Poland in a fully remote setup.In this role you will support Centralized Monitoring by configuring and maintaining systems setting up new studies and developing standard and bespoke monitoring function

Are you detail-oriented and passionate about supporting clinical research operations Join our team as an FSP Clinical Project Coordinator where youll play a key role in enabling regulatory workflows across clinical studies. This is a sponsor-dedicated office-based position in Vienna

Are you detail-oriented and passionate about supporting clinical research operations Join our team as an FSP Clinical Project Coordinator where youll play a key role in enabling regulatory workflows across clinical studies. This is a sponsor-dedicated office-based position in Vienna

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the East Coast Midwest & West Coast 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 t

Our FSP team is currently seeking Sr. CRA 2s with 4 years of monitoring residing in the East Coast Midwest & West Coast 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 t

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

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

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp