Emprego clinical research 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...

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, our company policies and procedures,...

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...

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, maintenance of...

Senior Clinical Data Manager – FSP / Oncology Experience Join to apply for the Senior Clinical Data Manager – FSP / Oncology Experience role at Fortrea. The Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management queries, from...

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 Managing...

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...

A global clinical research organization is seeking a Senior Clinical Data Manager to oversee and lead clinical data management projects. This role requires a university degree and 8 years of experience, including sponsor management. The successful candidate will manage vendor contracts and ensure data quality. The position offers a competitive compensation package, with options for office or...

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 Managing...

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...

A leading global clinical research provider is looking for a Clinical Trial Assistant in Lisbon, Portugal. The role involves supporting Clinical Research Associates and the Regulatory and Start-Up team by managing clinical documents, assisting with compliance tracking, and preparing necessary reports. Candidates should possess a high school diploma, at least 2 years of experience in this role,...

Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Responsibilities - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF))...

A leading global clinical research provider is seeking a Regulatory and Start Up Manager to oversee site activation and regulatory activities. This role requires at least 7 years of experience in scientific or clinical environments and proficiency in Portuguese for communication with the Competent Authority. The ideal candidate will possess strong negotiation and communication skills and a...

A leading global clinical research provider is seeking a Senior Psychometrician in Lisbon, Portugal. This role involves managing the psychometric evaluation of Clinical Outcome Assessment instruments used in clinical trials. The ideal candidate will possess a Master’s or PhD in a related field with extensive experience in the healthcare industry. Responsibilities include managing project...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master...

Location: EU-Wide (hybrid/remote) Real World Commercial Solutions to Create a Healthier World In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare...