Empleos de clinical study coordinator en Sevilla

Bring your clinical research expertise to a groundbreaking study and make a meaningful impact from day one.Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura.R&D Partners is seeking a Clinical Research Coordinator (CRC) to support clinical research activities at a study site in Seville, Spain. This role...

R&D Partners is seeking a Clinical Research Coordinator to support activities at a study site in Seville, Spain.Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.This role offers an opportunity to contribute to groundbreaking research in collaboration with a...

Overview In this role you lead full-service oncology clinical projects within a CRO setting, driving delivery across global trials and coordinating cross-functional teams. You will oversee client relationships, project scope, budgets, and timelines from proposal through study completion. You work closely with internal and external stakeholders to ensure...

Overview In this CRA role, you monitor oncology/hematology trials and ensure adherence to ICH-GCP, local regulations, and SOPs. You collaborate with the Regional Clinical Operations Manager to meet study milestones and maintain data quality. You identify gaps, propose CAPAs, and support site start-up and local expertise. You work across sites to drive...

Overview Join Precision for Medicine as a Clinical Project Manager/Senior CPM to lead end‐to‐end global oncology trials in a CRO environment. You will drive project delivery, manage cross‐functional teams, and maintain client relationships, budgets, and timelines from proposal through study completion. You'll ensure quality and coordination across...

Overview In this role you lead global clinical trial activities to ensure on-time delivery and high-quality results within Parexel's sponsor-driven environment. You guide cross‐functional trial teams, manage timelines and budgets, and ensure regulatory compliance across regions. You partner with internal and external stakeholders to translate strategy...

Overview In this role you will lead the configuration and deployment of eTMF, CTMS and related solutions for life sciences customers, ensuring alignment with regulatory and validation needs. You will guide design decisions, deliver training, and support customers through application validation and lifecycle activities. As a Senior Consultant you will...

Overview In this role you ensure robust clinical trial compliance at country and site levels within an oncology-focused research landscape. You work with country, regional, and global teams to safeguard patient safety, data integrity, and inspection readiness. You apply a risk-based approach to identify and manage compliance risks and influence study...

Overview As Global Study Manager (Oncology) you will lead interdisciplinary clinical programs from proposal to final deliverables, ensuring GCP compliance and financial performance. You'll act as the primary liaison with customers to launch, run, and close studies within contractual scopes. You'll guide cross-functional teams, manage timelines, and mentor...

Overview In this role you ensure high-quality clinical data for sponsor-led trials, working remotely across Poland, Spain or the UK. You will review patient data, resolve data inconsistencies, and support data-cleaning activities ahead of analyses, collaborating with cross-functional teams to meet GCP and protocol requirements. You will help maintain data...

[Last day to apply: Sunday, September 20]About us 🩺Legit.Health deploys computer vision and artificial intelligence medical devices to enable lifesaving diagnosis and therapies for visible diseases. Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone...

Overview In this role you will guide late-phase Hematology/Immunology trials as a sponsor-side Clinical Project Manager II. You'll coordinate with CROs and vendors, drive study timelines, and oversee documentation and risk management. This position offers global scope and a chance to shape pivotal studies within a mission-driven organization. ...

Overview In this Global Clinical Project Manager II role, you will support late-phase Hematology and Immunology trials for sponsor programs. You will liaise with CROs and vendors, keep the project team aligned on timelines, and contribute to study documents and risk templates. You'll drive end-to-end trial execution from start-up through close-out,...

(Last day to apply: Sunday, September 20) About us Legit.Health deploys computer vision and artificial intelligence medical devices to enable lifesaving diagnosis and therapies for visible diseases. Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone...

IQVIA is expanding its global network of Central Independent Raters (CIRs) to support a depression study. This 100% remote, project-based role requires about 10 hours per week as a freelance contract. Fluency in Spanish with good English is preferred, and a Master’s degree in psychology/psychiatry is ideal. Ideal candidates have 2–3 years of clinical...

(Last day to apply: Sunday, September 20) About us Legit.Health deploys computer vision and artificial intelligence medical devices to enable lifesaving diagnosis and therapies for visible diseases. Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone...

Overview In this role you will oversee site management, clinical and central monitoring to safeguard patient safety, data integrity, and regulatory compliance. You will manage activities from activation to closeout, coordinate with cross-functional teams, and apply risk-based approaches to keep trials on track. You will engage with investigators and sites,...

Overview In this role you drive late-phase oncology development by turning scientific strategy into executable clinical trials. You lead protocol execution, data quality, and cross-functional collaboration to produce decision-ready data that informs regulatory decisions. You will be a scientific expert across the therapeutic area, guiding investigators,...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.¿Listo para inscribirse? Antes de hacerlo, asegúrese de...

Overview In this CRA role, you monitor oncology/hematology trials and ensure adherence to ICH-GCP, local regulations, and SOPs. You collaborate with the Regional Clinical Operations Manager to meet study milestones and maintain data quality. You identify gaps, propose CAPAs, and support site start-up and local expertise. You work across sites to drive...