Empleos de clinical data en Zaragoza

IIS Aragon convoca una plaza para recién titulados con Máster oficial en Genética Molecular y/o Biología Molecular y Celular, y al menos dos años de experiencia en proyectos científicos relacionados con genética clínica y omics.Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta...

About usSunday, 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 everywhere.We are...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...

Parexel are currently recruiting for an experienced Global Patient and Site Engagement – Clinical Trial Liaison professional to join one of our growing sponsors in Spain .This will be a fully remote home-based position and is only open to applicants in the countries listed above.Some specifics about this advertised roleClinical Trial Site...

Overview As a Clinical Scientist Director in Early Development Oncology, you translate scientific strategy into actionable clinical execution in early-phase trials. You provide hands-on oversight of protocol execution, data quality, and medical data review to enable decision-ready data. You collaborate across cross-functional teams to align trials with...

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...

Iisaragon is seeking a Vocational Training Technician in research support with a Higher Level Vocational Training Certificate in Clinical Diagnostic Laboratory or equivalent. The role involves processing biological samples, maintaining clinical databases, and ensuring data integrity. Candidates should have five years of relevant experience.The work is...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, Customer...

Legit.Health seeks a Clinical Affairs Manager to own clinical evaluation and regulatory documentation end-to-end, collaborating with Quality, Regulatory, and Product Development while leading clinical conversations.You will build a network of consultants, design budgets for the clinical evidence department, manage data with traceability, and author SAP and...

Overview In this CRA II role, you will oversee clinical trial activities to ensure protocol and regulatory compliance across sites. You will work closely with site teams and cross-functional partners to monitor data integrity, patient safety, and trial progress. You’ll apply risk-based monitoring techniques and drive site performance improvements to...

Are you looking to be part of something special, like shaping the future of healthcare?We are looking for a Data Engineer to help build, test, and optimise the pipeline powering our analytics, reporting, and data products.This is a role with real ownership to contribute to the next generation of our platform.If this sounds like you, keep reading!At Semble,...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong...

Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Madrid, Spain Full time R We are looking for a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for biostatisticians or data scientists with a strong interest...

Overview As a field-based medical expert, you will shape medical strategy and drive data generation in your disease area. You'll build long-term partnerships with TAEs and investigators to deliver value to healthcare professionals, while leading field medical plan execution in collaboration with the Country Medical Manager. You'll translate insights into...

Overview In this remote role, you provide Quality Assurance support for Global Medical Affairs Vendor & Third-Party Management, handling quality events, investigations, CAPAs, audits, and due diligence. You collaborate with cross-functional partners to ensure compliance, risk management, and audit readiness across third-party activities. You will lead...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. Your expertise shapes content strategy, standards, and processes for global regulatory submissions. This is a hands-on writing leadership role with a clear focus on precision, deadlines, and impact on...

Overview In this remote role, you provide Quality Assurance support for Global Medical Affairs Vendor & Third-Party Management, handling quality events, investigations, CAPAs, audits, and due diligence. You collaborate with cross-functional partners to ensure compliance, risk management, and audit readiness across third-party activities. You will lead...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. Your expertise shapes content strategy, standards, and processes for global regulatory submissions. This is a hands-on writing leadership role with a clear focus on precision, deadlines, and impact on...