Emprego clinical research associate Oeiras

Clinical Research Associate 2 - Based in Portugal IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide....

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 bio/pharma sector. Candidates must be fluent in...

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 project plans, as assigned. Summary Of...

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 regulations, our company policies and...

Sr. Associate, Clinical Applications Services & Support page is loaded## Sr. Associate, Clinical Applications Services & Supportremote type: Remote - Sales / Field services positionlocations: Oeiras, Portugaltime type: Full timeposted on: Posted Todaytime left to apply: End Date: January 20, 2027 (30+ days left to apply)job requisition id: R-2025-44180At Alcon, we are driven by the meaningful...

Overview At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an...

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive...

A global clinical research provider is seeking a Clinical Research Associate 2 based in Portugal. The role involves performing site selection and monitoring visits, supporting subject recruitment, and ensuring regulatory compliance. Candidates must have a relevant university degree and a minimum of two to four years' experience in monitoring. Excellent communication skills in Portuguese and...

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 regulations, our company policies and...

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 designated clinical projects as a Local Project...

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 closeout of clinical sites,...

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive...

Clinical Research Associate - based in Porto Join to apply for the Clinical Research Associate - based in Porto role at IQVIA. 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,...

A leading global provider of clinical research services is looking for a Clinical Research Associate based in Porto. This entry-level, full-time role requires performing site selection, initiation, monitoring, and close-out visits while supporting the development of subject recruitment plans. Applicants should hold a relevant university degree and possess strong monitoring experience, excellent...

Clinical Research AssociateYour 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 Harmonization guidelines Managing progress by...

Clinical Research AssociateYour 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 Harmonization guidelines Managing progress by...

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 regulations, our company policies and...

Job Description Summary Essential Functions: Manages multiple teams of professional-level employees and/or managers responsible for successful execution of Managed Services client projects at IQVIA. Develops and communicates objectives and priorities and coordinates strategic planning, research, and the tactical development, implementation, and management of deliverables. Manages the...

Job Description Summary Essential Functions: Manages multiple teams of professional-level employees and/or managers responsible for successful execution of Managed Services client projects at IQVIA. Develops and communicates objectives and priorities and coordinates strategic planning, research, and the tactical development, implementation, and management of deliverables. Manages the...

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 Harmonization guidelines -...