Study - 16+ vagas

About us<\/b><\/span> <\/p> We are a CRO company located in Lisbon that works for the Pharmaceutical and Medical industry. Our IT, Scientific and Language Affairs areas help our clients achieve their goals and improve healthcare around the globe.<\/span> <\/p> Our Scien

A leading AI healthcare company is looking for a Clinical Study Manager to oversee the operational execution of clinical trials. This role demands strong skills in project management to ensure studies are delivered on time and within budget. The candidate will manage timelines, coordinate with vario

A leading AI healthcare company is looking for a Clinical Study Manager to oversee the operational execution of clinical trials. This role demands strong skills in project management to ensure studies are delivered on time and within budget. The candidate will manage timelines, coordinate with vario

About The Job At Alignerr, we partner with the world’s leading AI research teams and labs to build and train cutting-edge AI models. We are hiring Clinical Study Managers to help oversee the operational execution of clinical trials, ensuring that studies are delivered on time, within budget, and to

Coordinate clinical studies, liaise with healthcare professionals and patients, and ensure data accuracy.

Coordinate clinical studies, liaise with healthcare professionals and patients, and ensure data accuracy.

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US

A leading global provider of clinical research services is looking for a Study Start-Up Lead in Portugal. This role involves planning and executing global study start-up activities, coordinating with health authorities, and ensuring timely site activation to meet recruitment goals. Ideal candidates

Manage clinical trials operations, budgets, and timelines for AI research projects. Requires experience in trial management and vendor coordination.

Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet co

A leading global clinical research provider is seeking a Project Lead in Lisbon, Portugal. This role involves managing clinical studies, liaising with clinical teams, and ensuring successful project delivery. The ideal candidate will have over 7 years of clinical research experience, with a solid ba

A leading pharmaceutical company in Porto is looking for a Clinical Research Physician (Temporary) to design and medically monitor clinical studies. You'll need a Degree in Medicine and excellent communication skills. Experience in the neurosciences area is preferred. This role requires strong organ

A leading AI healthcare company is looking for a Clinical Study Manager to oversee the operational execution of clinical trials. This role demands strong skills in project management to ensure studies are delivered on time and within budget. The candidate will manage timelines, coordinate with vario

The Study Start-Up (SSU) Lead plans and executes global SSU activities to ensure timely trial document and task completion to enable country HA (Health Authorities) and Ethics Committee submissions and site activation to meet ambitious recruitment plans. The Study Start-Up Lead works collaboratively

CTI Clinical Trial Services

Feasibility Study Specialist I (Please note this role can be located in any country where CTI has a legal entity) Job Purpose / Summary Assists in analyzing and researching institutions and Investigators via CTI Feasibility Database, Data Assets and Business Intelligence to develop site, investigato

Join The CTI Team

What You'll Do: Regulatory Submission Management Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics com