Full-time hours
What you'll do The Associate Director, Global Health Economics & Outcomes Research (GHEOR) Analytics, develops and implements HEOR Analytics strategy, including conceptualizing real-world evidence studies, identification of data sources, study conduct and execution of publication plan. The incumbent will engage in hands ...
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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- Remoto
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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 ...
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, ...
Full-time hours
... appreciate your honesty and professionalism. KNOWLEDGE, SKILLS AND ABILITIES: - Understanding of GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research. - Advanced knowledge of statistical methods used in the design and analysis of Phase I-IV clinical trials. - Experience with SAS Base and SAS Stat. ...
Full-time hours
... crucial field for the industry Skills & Experience - Proven analytical, interpretative and problem-solving skills - Proven interest in patient-centered-related research and topics (e.g., Clinical Outcome Assessment, Patient-Reported Outcome, electronic implementation a plus). - Strong interpersonal and relationship building ...
... scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand ...
Spain, Barcelona
Ver vacanteFull-time hours
About the role The Clinical Marketing - Microbiology develops and executes clinical marketing strategies that strengthen the clinical value, scientific evidence, and differentiated positioning of the Microbiology in Iberia. Working closely with the Product Managers, the role converts clinical data, realworld insights, and ...
Full-time hours
... Practices. - Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate ...
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- Híbrido
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SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in Spain, Portugal, France and Ireland. SOLTI focuses its efforts on developing cutting-edge ...
Spain, Barcelona
Ver vacanteFull-time hours
About the job JOB DESCRIPTION: Main Purpose of the Role • This is a sales position where the individual is responsible for servicing the current customer base, increasing sales within that base and establishing new accounts.
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Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time 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 activities, scientific and medical ...
Spain, Pamplona
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Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time 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 activities, scientific and medical ...
- Híbrido
- Tiempo completo
- Contrato
Permanent contract
... experience producing clear written deliverables and presenting information to internal or 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 ...
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Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time 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 activities, scientific and medical ...
- Híbrido
- Presencial
- Tiempo completo
Full-time hours
... publications in leading ML and clinical AI journals. - Serve as a technical mentor and thought partner for Associate Directors and Senior Data Scientists within the Clinical AI team; promote scientificrigour, reuse, and a culture of learning in public. - Contribute to the broader AISI AI for Clinical Development strategy, including ...
- Remoto
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- Contrato
Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Full-time 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 activities, scientific and medical ...
Spain, Alacante
Ver vacante- Remoto
- Híbrido
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Full-time hours
... Degree in natural or biological sciences, or equivalent combination of education and relevant experience. - Approximately 5 years of experience in GCP, GPvP, clinical research, pharmaceutical industry, health authority or equivalent environment. - 1-2 years of GCP auditing experience preferred. - Strong knowledge of applicable ...
Full-time hours
... software developers, including compiler teams, to facilitate the adoption of novel architectures. - Supporting scientific communities, industrial partners, and research projects in testing novel architectures and comparing results with state-of-the-art HPC systems. The team is seeking a postdoctoral researcher to lead activities ...
- Presencial
- Tiempo completo
€48,000 - €68,000 a year
About the role We are seeking an experienced Senior Regulatory Affairs Specialist to join our Clinical Operations team in Spain. This is a Full-time, on-site position where you will play a crucial role in ensuring compliance with regulatory requirements across our clinical trial operations. You will be responsible for managing ...