Fortrea

Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.Key ResponsibilitiesConduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.Ensure patient safety data integrity and p

Here at Fortrea we are recruiting a junior Clinical Research Associate I to work within our multisponsor clinical team.Key ResponsibilitiesConduct site monitoring activities including prestudy initiation routine monitoring and closeout visits.Ensure patient safety data integrity and p

Job Overview:Site Navigators play 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 this r

Job Overview:Site Navigators play 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 this r

Are you a proposal leader who thrives in a fastpaced clientdriven environmentsomeone who enjoys developing and supporting a highperforming team while remaining closely connected to complex strategic opportunitiesWe are hiring a Manager Proposal Management to join Fortreas Enterprise C

Are you a proposal leader who thrives in a fastpaced clientdriven environmentsomeone who enjoys developing and supporting a highperforming team while remaining closely connected to complex strategic opportunitiesWe are hiring a Manager Proposal Management to join Fortreas Enterprise C

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Associate Director PSS Remote based USWe are seeking an accomplished Associate Director with patient safety solutions expertise who is seasoned in aggregate writing and leadership. The Associate Director PSS will manage regional pharmacovigilance operations across Europe Asia-Pacifi

Senior Coding Specialist Mexico Candidates must be based in MexicoAre you passionate about medical coding quality and clinical data integrity Were looking for a Senior Coding Specialist based in Mexico to support highquality compliant clinical trial data across global studies.What yo

Senior Coding Specialist Mexico Candidates must be based in MexicoAre you passionate about medical coding quality and clinical data integrity Were looking for a Senior Coding Specialist based in Mexico to support highquality compliant clinical trial data across global studies.What yo

Job Overview:Responsibility for the annual country specific QC plan monitoring and coordinating the implementation and execution of QC plan in the respective country/US region according to the Client Standard Operating Procedures and ICH Guidelines and GCP. Responsibility for the mana

Job Overview:Responsibility for the annual country specific QC plan monitoring and coordinating the implementation and execution of QC plan in the respective country/US region according to the Client Standard Operating Procedures and ICH Guidelines and GCP. Responsibility for the mana

Job Overview:Were seeking a Workday Configuration Developer Manager to assist with design and endtoend solutioning across our Workday PATT portfolioSummary of Responsibilities:Configure andmaintainWorkday Payroll Absence and Time Tracking modules to meet complex business requirements.

Job Overview:Were seeking a Workday Configuration Developer Manager to assist with design and endtoend solutioning across our Workday PATT portfolioSummary of Responsibilities:Configure andmaintainWorkday Payroll Absence and Time Tracking modules to meet complex business requirements.

Job Overview:Were seeking a Workday Configuration Developer Manager to assist with design and endtoend solutioning across our Workday PATT portfolioSummary of Responsibilities:Configure andmaintainWorkday Payroll Absence and Time Tracking modules to meet complex business requirements.

Job Overview:Were seeking a Workday Configuration Developer Manager to assist with design and endtoend solutioning across our Workday PATT portfolioSummary of Responsibilities:Configure andmaintainWorkday Payroll Absence and Time Tracking modules to meet complex business requirements.

Were hiring: Clinical Data Specialist Clinical Data Management (Mexico) Location: Mexico (candidates must be currently based in Mexico)Do you enjoy turning complex lab data into clean reliable clinical insights Join our Clinical Data Management team as a Clinical Data Specialist and

Were hiring: Clinical Data Specialist Clinical Data Management (Mexico) Location: Mexico (candidates must be currently based in Mexico)Do you enjoy turning complex lab data into clean reliable clinical insights Join our Clinical Data Management team as a Clinical Data Specialist and

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

Job Overview:The Physician Assistant will provide an information service and knowledge base on the clinical aspects of clinical trials in Clinical addition he/she may act as a sub-investigator.Summary of Responsibilities:Perform physical examinations/medical histories and other parti

Job Overview:The Physician Assistant will provide an information service and knowledge base on the clinical aspects of clinical trials in Clinical addition he/she may act as a sub-investigator.Summary of Responsibilities:Perform physical examinations/medical histories and other parti

Summary of ResponsibilitiesAs a Clinical Research Associate (CRA II / Senior CRA I) you will be responsible for the endtoend management and monitoring of clinical trial sites ensuring studies are conducted in compliance with Fortrea SOPs ICHGCP guidelines and applicable regulatory req

Summary of ResponsibilitiesAs a Clinical Research Associate (CRA II / Senior CRA I) you will be responsible for the endtoend management and monitoring of clinical trial sites ensuring studies are conducted in compliance with Fortrea SOPs ICHGCP guidelines and applicable regulatory req

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 groups 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 groups or as stand- alone business. Responsible for providing

Job Overview:The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG) expected to leverage their Research and Development experience Therapeutic Area (TA) experience and operational study execution experience to sustainably grow and maintain a port

Job Overview:The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG) expected to leverage their Research and Development experience Therapeutic Area (TA) experience and operational study execution experience to sustainably grow and maintain a port

Job Overview:The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG) expected to leverage their Research and Development experience Therapeutic Area (TA) experience and operational study execution experience to sustainably grow and maintain a port

Job Overview:The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG) expected to leverage their Research and Development experience Therapeutic Area (TA) experience and operational study execution experience to sustainably grow and maintain a port

Job Overview:The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG) expected to leverage their Research and Development experience Therapeutic Area (TA) experience and operational study execution experience to sustainably grow and maintain a port

Job Overview:The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG) expected to leverage their Research and Development experience Therapeutic Area (TA) experience and operational study execution experience to sustainably grow and maintain a port

***Previous experience supervising a team within a CRO strongly preferred ***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 Supervisor Clinical Operations to interact directl

***Previous experience supervising a team within a CRO strongly preferred ***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 Supervisor Clinical Operations to interact directl

As one of the largest Clinical Research Organizations globally we operate Early Phase Clinical Research Units in both the United States and the United Kingdom. We are currently seeking a Clinical Data Monitor to join our Dallas TX team in a fulltime officebased role.The Clinical Data

As one of the largest Clinical Research Organizations globally we operate Early Phase Clinical Research Units in both the United States and the United Kingdom. We are currently seeking a Clinical Data Monitor to join our Dallas TX team in a fulltime officebased role.The Clinical Data

Remote job UK-wide or Hybrid if you live in/close to our Leeds officeAccountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client.T

Remote job UK-wide or Hybrid if you live in/close to our Leeds officeAccountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and financial compliance at a country operations level at the client.T