9k
... sustainable development. Ready to become a #Challenger? What are we looking for? Planning, designing, organization, supervision of conduct and reporting of clinical trial contracted to Clinical Research Organizations (CRO) to enable studies execution within the planned timelines and in compliance with current GCP and other ...
Spain, Guadalajara
Ver vacante€140,000 - €200,000 a year
... pre-case planning, CT analysis and pre- and post-procedure recommendations to support optimal clinical outcomes. - Maintain in-depth knowledge of existing DurAVR clinical data and the evolving structural heart evidence landscape. - Support the Clinical and Regulatory Operations teams with site communications, data compliance ...
9k
... sustainable development. Ready to become a #Challenger? What are we looking for? Planning, designing, organization, supervision of conduct and reporting of clinical trial contracted to Clinical Research Organizations (CRO) to enable studies execution within the planned timelines and in compliance with current GCP and other ...
Spain, Guadalajara
Ver vacanteFull-time hours
... structure and limitations of various types of real-world databases, and experience in working with large EMR or claims database are preferred. - Experience with big data science, machine learning, AI models. - Knowledge of clinical trials, and experience in analyzing and interpreting clinical trial data. - Excellent written and ...
€70,000 a year
... forecasts and activity reports to management. - Collaborate with operations, quality assurance, and project management teams to ensure a smooth onboarding of new clinical supplies projects. - Analyze competitor offerings and their pricing strategies within the secondary packaging and clinical logistics sector. What you'll get ...
Full-time hours
... performs required administrative sales duties, e.g., filing expense account reports, scheduling appointments, and making travel plans. - Maintain business operations in accordance with corporate policies in respect to pricing. quotes, credit terms, expense reporting and Quality guidelines. - Follow and share the best practices ...
- Remoto
- Tiempo completo
- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Employment type: Full-time Role Summary We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research ...
- Remoto
- Tiempo completo
- Contrato
... experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including ...
Spain, Pamplona
Ver vacante- Remoto
- Tiempo completo
- Contrato
... experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including ...
- Remoto
- Tiempo completo
- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Employment type: Full-time Role Summary We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist , you will support clinical research ...
Spain, Vitoria
Ver vacante- Híbrido
- Tiempo completo
- Contrato
Permanent contract
... external stakeholders. Nice to have - Competitive intelligence or market research background in life sciences. - Experience developing software products for clinical trial design, operations, or analytics. What you'll get - Private Medical Insurance or Health Cash plan - Generous Pension Plan contribution rates - Income ...
- Remoto
- Tiempo completo
- Contrato
... experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including ...
- Remoto
- Tiempo completo
- Contrato
... experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Support the preparation and execution of Clinical Investigations and Performance Studies - Assist with monitoring‑support activities and data‑related tasks - Contribute to scientific and medical writing, including ...
Spain, Alacante
Ver vacante... -Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date - Supports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR) - Supports the vendor selection, scope development, ...
Full-time hours
... literacy and adoption initiatives across R&D. This role works across the AI Literacy team, to ensure a cohesive and impactful experience for R&D employees. The Associate Director will bring a strong clinical and scientific perspective while helping shape content, identify high-value use cases for tools, engage stakeholders, ...
... Hybrid Division: Development Data, Digital & IT (DDIT) Function: Global Clinical Operations (GCO) About the Role At Novartis, we are reimagining medicine through data, digital, AI, and advanced technologies. We are seeking an experienced Associate Director, Clinical Solution Architecture - AI & Digital Platforms to lead the ...
Spain, Barcelona
Ver vacante... ecosystem. You will shape the integration architecture connecting key clinical systems - including Electronic Data Capture, electronic Trial Master File, and Clinical Trial Management systems - while ensuring data integrity, security, and compliance with GxP validation standards. Partnering with Clinical Operations, Data ...
Spain, Mollet del Vallés
Ver vacante... ecosystem. You will shape the integration architecture connecting key clinical systems - including Electronic Data Capture, electronic Trial Master File, and Clinical Trial Management systems - while ensuring data integrity, security, and compliance with GxP validation standards. Partnering with Clinical Operations, Data ...
Spain, Mollet del Vallés
Ver vacante- Remoto
- Híbrido
- Presencial
- Tiempo completo
- Contrato
€63,000 - €65,000 a year
... Ophthalmology Qualifications - Bachelor's degree in Life Sciences, Clinical Research, Nursing, Pharmacy, or another health-related field. - Minimum of 5 years of clinical research experience, including significant experience as a Clinical Research Associate (CRA) with independent on-site monitoring responsibilities. - Minimum ...
de 50000 a 85000 €/año
... such as Veeva Vault, ePharmaSolutions, PhlexEview, WingSpan, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, BioClinica CTMS, IMPACT CTMS, Medidata CTMS, GoBalto, or other clinical technologies - Life-science or computer science-related degree - SaaS/Cloud experience - Experience in demoing software applications ...