التالي
Job Overview:Responsible to provide support lab compliance activities.Summary of Responsibilities:These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities skills and duties as individual contributor g
Job Overview:Responsible to provide support lab compliance activities.Summary of Responsibilities:These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities skills and duties as individual contributor g
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 Lab Technician to interact directly with our healthy volunteer participants while learning to read clinical research protocol
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 Lab Technician to interact directly with our healthy volunteer participants while learning to read clinical research protocol
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 Research Nurse / Open to RNs LPNs or Paramedics to lead and support our Clinical Pharmacology Start-up team in initiating Ear
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 Research Nurse / Open to RNs LPNs or Paramedics to lead and support our Clinical Pharmacology Start-up team in initiating Ear
Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile
Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile
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 to interact directly with our healthy volunteer participants while learning to read clinical r
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 to interact directly with our healthy volunteer participants while learning to read clinical r
A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha
A career in Clinical Research with Fortrea: from the hospital ward to the world.If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pha
Fortrea
Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments
Summary of Responsibilities:Perform the role of the Lead Statistical Programmer.Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments
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
Are you ready to make an impact in clinical research while leveraging your administrative expertise Join our dynamic FSP team in Vienna as a and help shape the future of clinical development at Fortrea.Why this role matters: You will play a key role in supporting clinical trial operat
Are you ready to make an impact in clinical research while leveraging your administrative expertise Join our dynamic FSP team in Vienna as a and help shape the future of clinical development at Fortrea.Why this role matters: You will play a key role in supporting clinical trial operat
Fortrea
Job Overview:May support Lead Data Manager (LDM) with the review maintenance and update of external vendor data received from central vendor or local laboratories. Working to ensure company SOPs (or sponsor if applicable) guidelines and global standards are followed to maintain data i
Job Overview:May support Lead Data Manager (LDM) with the review maintenance and update of external vendor data received from central vendor or local laboratories. Working to ensure company SOPs (or sponsor if applicable) guidelines and global standards are followed to maintain data i
