Experienced Clinical Research Associate

Senior Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...

Senior Clinical Research AssociateYour responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...

A global clinical research organization seeks a Clinical Research Associate 2 in Portugal. Responsibilities include site monitoring, ensuring patient safety, and compliance with regulatory guidelines in clinical studies. The ideal candidate should have a degree in a health-related field, at least one year of CRA experience, and strong English communication...

Job Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local...

Clinical Research Associate 2 - FSO Model - Portugal Join to apply for the Clinical Research Associate 2 - FSO Model - Portugal role at Fortrea. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Ensures the implementation of...

Join Fortrea as a SR Clinical Research Associate - Drive Clinical Excellence in Oncology Trials. This role is for upcoming future opportunities that may arise at Fortrea. As a SRCRA, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You’ll coordinate...

A clinical research organization is seeking a Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols. You will manage site activities across Portugal, ensuring adherence to regulations and quality standards. The role requires a Bachelor’s degree and a minimum of 3 years direct site management experience in the...

Job Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local...

Job DescriptionWe are seeking a highly skilledClinical Research Associate (CRA)to lead performance and compliance for assigned protocols and sites withinPortugal - Zona Norte. Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations,...

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 aspects of study site monitoring including routine monitoring and...