Fortrea

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

Job Overview:The Senior Manager Site and Patient Engagement Delivery leads integrated recruitment retention site engagement and partnership strategies across assigned studies and research partner relationships ensuring patient-focused delivery stronger site performance effective vendo

Job Overview:The Senior Manager Site and Patient Engagement Delivery leads integrated recruitment retention site engagement and partnership strategies across assigned studies and research partner relationships ensuring patient-focused delivery stronger site performance effective vendo

Job Overview:The Senior Manager Site and Patient Engagement Delivery leads integrated recruitment retention site engagement and partnership strategies across assigned studies and research partner relationships ensuring patient-focused delivery stronger site performance effective vendo

Job Overview:The Senior Manager Site and Patient Engagement Delivery leads integrated recruitment retention site engagement and partnership strategies across assigned studies and research partner relationships ensuring patient-focused delivery stronger site performance effective vendo

We are recruiting for multisponsor team in Greece and are currently seeking to hire a Senior CRA I with a permanent and full-time contract. Our positions offer excellent exposure to a range of disease areas and a real opportunity for career progression and promotion in time.What if yo

We are recruiting for multisponsor team in Greece and are currently seeking to hire a Senior CRA I with a permanent and full-time contract. Our positions offer excellent exposure to a range of disease areas and a real opportunity for career progression and promotion in time.What if yo

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Job Overview:Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US EU Japan and ROW health authorities and oversight of the same as applicable.Summary of Responsibilities:These statements are intended to describe the

Site Budget & Contract Lead (Full-Time Permanent Remote) - Sponsor dedicatedWe are currently seeking an experienced Site Budget & Contract Lead to join our team in a full-time permanent remote position. This is an exciting opportunity for a clinical research professional who enjoys le

Site Budget & Contract Lead (Full-Time Permanent Remote) - Sponsor dedicatedWe are currently seeking an experienced Site Budget & Contract Lead to join our team in a full-time permanent remote position. This is an exciting opportunity for a clinical research professional who enjoys le

What if the skills youve built in data entry could help bring new medicines to lifeFortreas 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 enjoy working wi

What if the skills youve built in data entry could help bring new medicines to lifeFortreas 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 enjoy working wi

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

Summary of Responsibilities:Supports or manages all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for opportunities as assigned.Responsible for managing opportunities of low to medium complexity.Shadow and/or assist mo

Summary of Responsibilities:Supports or manages all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for opportunities as assigned.Responsible for managing opportunities of low to medium complexity.Shadow and/or assist mo

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

Were excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.As a CRA2 you will play a key role in man

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

Are you ready to take the next step in your clinical research career and transition into a Clinical Research Associate roleWe are looking for motivated professionals with experience as a Study Nurse Study Coordinator Clinical Trial Assistant (CTA) or In-House CRA who are eager to move

Are you ready to take the next step in your clinical research career and transition into a Clinical Research Associate roleWe are looking for motivated professionals with experience as a Study Nurse Study Coordinator Clinical Trial Assistant (CTA) or In-House CRA who are eager to move

Summary of Responsibilities:Provide Statistical Programming support for clinical trial projects.Develop validate and maintain SAS programs and outputs for the management analysis and reporting of clinical trial data.Develop and maintain data transfer programs in accordance with client

Summary of Responsibilities:Provide Statistical Programming support for clinical trial projects.Develop validate and maintain SAS programs and outputs for the management analysis and reporting of clinical trial data.Develop and maintain data transfer programs in accordance with client

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 (location: Switzerland Home-based) you will play a pivotal role in coordinating site start-up activities mana

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 (location: Switzerland Home-based) you will play a pivotal role in coordinating site start-up activities mana

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

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

Job Overview: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 ensuring regulatory submissions are complet

Job Overview: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 ensuring regulatory submissions are complet

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

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

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator I in Germany or Austria youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.Key ResponsibilitiesAssist wi

Join Fortreas mission to transform clinical trials and improve patient outcomes.As a Study Start Up Site Navigator I in Germany or Austria youll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.Key ResponsibilitiesAssist wi