Fortrea

Fortrea is hiring for Call Center Representatives On-Call to recruit volunteer participants for our Phase 1 normal healthy volunteer studies.We have full-time part-time and on-call positions available.Training is on-site in our Dallas clinic for 4 weeks Monday - Friday from 8am-5pm CD

Fortrea is hiring for Call Center Representatives On-Call to recruit volunteer participants for our Phase 1 normal healthy volunteer studies.We have full-time part-time and on-call positions available.Training is on-site in our Dallas clinic for 4 weeks Monday - Friday from 8am-5pm CD

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:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience and level of contribution which they can mak

Job Overview:The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience and level of contribution which they can mak

What if your marketing expertise was the reason a new drug reaches patients fasterFORTREA IN LEEDS WHERE MEDICAL BREAKTHROUGHS BEGINAt Fortrea our world-class Clinical Research Unit in Leeds (just a short walk from the train station) is a 65000 ft² 100-bed facility dedicated to Early

What if your marketing expertise was the reason a new drug reaches patients fasterFORTREA IN LEEDS WHERE MEDICAL BREAKTHROUGHS BEGINAt Fortrea our world-class Clinical Research Unit in Leeds (just a short walk from the train station) is a 65000 ft² 100-bed facility dedicated to Early

Apprentice SEOExperience Required: 0 - 1 yearLocation: Bangalore (office based)Department: Digital Marketing TeamAbout the RoleWe are looking for an enthusiastic motivated and detail-oriented SEO Apprentice to join our dynamic Digital Marketing team in Bangalore. This apprenticeship

Apprentice SEOExperience Required: 0 - 1 yearLocation: Bangalore (office based)Department: Digital Marketing TeamAbout the RoleWe are looking for an enthusiastic motivated and detail-oriented SEO Apprentice to join our dynamic Digital Marketing team in Bangalore. This apprenticeship

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

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:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Were Hiring: IT Audit Lead Make an Impact Across the Enterprise! Are you a strategic thinker with a passion for technology risk and controls Were looking for an experienced IT Audit professional to lead and execute enterprise-level IT and integrated audits from cloud security and IT

Were Hiring: IT Audit Lead Make an Impact Across the Enterprise! Are you a strategic thinker with a passion for technology risk and controls Were looking for an experienced IT Audit professional to lead and execute enterprise-level IT and integrated audits from cloud security and IT

Job Overview:Line manage PSS staff including performance reviews human resource issues and assist Senior PSS Management in assigning resources to projects.Manage the overall PSS operations associated with products including the entire adverse events process; which may include safety d

Job Overview:Line manage PSS staff including performance reviews human resource issues and assist Senior PSS Management in assigning resources to projects.Manage the overall PSS operations associated with products including the entire adverse events process; which may include safety d

Develop in conjunction with the Global Feasibility Lead the initial site list for feasibility and site identificationFull oversight of the Feasibility/Site identification process: survey development and programming local resource training and oversight oversight of site outreach proce

Develop in conjunction with the Global Feasibility Lead the initial site list for feasibility and site identificationFull oversight of the Feasibility/Site identification process: survey development and programming local resource training and oversight oversight of site outreach proce

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:The In-House Clinical Research Associate (IHCRA I) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA I shall reflect their experience and level of contribution wh

Job Overview:The In-House Clinical Research Associate (IHCRA I) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA I shall reflect their experience and level of contribution wh

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:Serve as a member of the project team with primary responsibility for clinical data review query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications and project timelines and producti

Job Overview:Serve as a member of the project team with primary responsibility for clinical data review query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications and project timelines and producti

Join Our Proposal Management Team! - Hybrid Role - Leeds UK Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehensi

Join Our Proposal Management Team! - Hybrid Role - Leeds UK Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehensi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

***Must possess at least 3-5 years of people management/direct reports experience.***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 Clinical Operations Supervisor II to int

***Must possess at least 3-5 years of people management/direct reports experience.***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 Clinical Operations Supervisor II to int

Join Our Proposal Management Team! Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehension and writing skills to

Join Our Proposal Management Team! Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehension and writing skills to