Fortrea

Fortrea is seeking Ophthalmology Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 2 years of experience. Prior monitoring experience required. Remote US or Canada based. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research

Fortrea is seeking Ophthalmology Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with 2 years of experience. Prior monitoring experience required. Remote US or Canada based. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research

Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5 years of global project management experience with mandatory experience in phase I. Candidates must be based in the United States or Canada. Job Overview:At times working under

Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5 years of global project management experience with mandatory experience in phase I. Candidates must be based in the United States or Canada. Job Overview:At times working under

Job Overview: The Executive and Equity Compensation Manager serves as a key subject matter expert responsible for the administration governance analysis and ongoing support of the Companys executive and equity compensation programs. This role partners closely with Human Resources Lega

Job Overview: The Executive and Equity Compensation Manager serves as a key subject matter expert responsible for the administration governance analysis and ongoing support of the Companys executive and equity compensation programs. This role partners closely with Human Resources Lega

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

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

At Fortrea we believe in improving lives through the power of science collaboration and innovation. As a global CRO partner we support mission-driven sponsors in bringing new therapies to the patients who need them.Were now hiring a Study Start-Up Lead to join a sponsordedicated team

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

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a CRF Specialist to be responsible for transcribing and managing study data ensuring accuracy and collaborating with various st

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a CRF Specialist to be responsible for transcribing and managing study data ensuring accuracy and collaborating with various st

Our FSP team is currently seeking a CRA 2 on the West Coast or Central with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for particip

Our FSP team is currently seeking a CRA 2 on the West Coast or Central with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.WHAT YOU WILL DOYou will utilize your skills knowledge and clinical judgement to provide a high standard of care for particip

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

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

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: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: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: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

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: Serve as overall FSP customer expert and strategic business partner. Work closely with sales responsible for developing and expanding new FSP business opportunities with customers. Provide consultative FSP support to potential and existing clients. Establish grow and hel

Job Overview: Serve as overall FSP customer expert and strategic business partner. Work closely with sales responsible for developing and expanding new FSP business opportunities with customers. Provide consultative FSP support to potential and existing clients. Establish grow and hel

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

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

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

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