Empleos de Fortrea en Argentina

Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities. · ...

Summary Of Responsibilities · Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. · Conducts site monitor ...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and tech ...

The Logistics Manager is responsible for coordinating and overseeing aspects of logistics related to Clinical and Ancillary Supplies services. · ...

The role of the Lead Statistical Programmer includes planning, executing and overseeing all programming activities on a study. This involves developing and maintaining SAS programs to create SDTM and ADaM datasets and TFLs.Mentor less-experienced programmers in the processes arou ...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical ...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and tech ...

Contact with investigative sites during study maintenance and site startup activities. Responsible for collection of documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within timelines. Develop awareness of regulatory legislation in assigned countries ...

Summary of Responsibilities: · Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. · Conducts site monito ...

The Senior CRA I is responsible for site monitoring and site management. This includes routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; · Ensure the study staff who will conduct the pr ...