Empleos de clinical data en Sevilla

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...

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 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...

Clinical Pharmacist Facilitator – Hawkes Bay Fallen Soldiers Hospital (Full Time, Permanent)Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud.Support safer, wiser prescribing and improve medicines management across primary care in Te Matau a Māui.Health New Zealand...

Seeking a Clinical Affairs Manager for a Medtech SaaS startup. Responsibilities include designing and defending clinical evidence strategy, authoring regulatory documentation for EU and FDA submissions, and managing clinical data and audits.

Overview In this role you will draft, negotiate, and finalize complex clinical site contracts for sponsor-driven studies, ensuring timely execution and accurate data in CMS. You will partner with CBO, GCO, Legal, and site teams to manage contract lifecycles, budgets, and compliance in a fast-paced environment. You will drive timely deliverables, quality...

Walker Cole International is exclusively supporting a well-established global Contract Research Organisation, with over 4 decades in the clinical research market, in the search for a Director of Business Development to lead their commercial expansion into Europe. This is a rare opportunity to build a European business development function from the ground up,...

[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...

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...

(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...

(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 drive end-to-end global clinical trial management on sponsor-supported programs, ensuring timely delivery and regulatory readiness. You will collaborate with cross-functional teams to oversee trial timelines, budgets, site feasibility, vendor management, and supply planning. You'll apply your therapeutic-area expertise in...

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,...

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 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,...

A global clinical research organization is seeking a Clinician Rater in Alcalá de Guadaíra, Spain. This role involves managing clinical assessments, developing training materials, and reviewing data for various projects. Ideal candidates should possess a Master's degree in a healthcare-related field and at least three years of clinical experience. Strong...

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...

A global clinical research organization is seeking a Clinician Rater in Alcalá de Guadaíra, Spain. This role involves managing clinical assessments, developing training materials, and reviewing data for various projects. Ideal candidates should possess a Master's degree in a healthcare-related field and at least three years of clinical experience. Strong...