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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
Ver vacante- Remoto
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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 ...
- Remoto
- Tiempo completo
- 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 ...
- Remoto
- Tiempo completo
- 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
- Tiempo parcial
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Part-time hours
... overseeing the following assessments: MINI and MADRS Ideal Background - Master's degree in Psychology, Psychiatry or a related field - min of 2-3 years of clinical experience following graduation - min of 2-3 years of experience working in clinical trials - Strong interviewing and assessment skills - Fluent Spanish, good ...
Fully remote
... take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our ...
Fully remote
... take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our ...
Fully remote
... process improvement initiatives from assessment and design through implementation and effectiveness evaluation within a CRO environment. - Strong knowledge of clinical trial operations, clinical monitoring, site management, and cross-functional trial delivery processes. - Strong knowledge of ICH-GCP, regulatory expectations, ...
... including Microsoft Office applications [solid excel/power point knowledge]. Nice to have - Clinical Trials experience preferred (central nervous system (CNS) trials experience would be a plus). Additional information IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence ...
Spain, Barcelona
Ver vacanteFull-time hours
... communicating with all levels of personnel and participating in collaborative work team (locally and globally). - Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. - Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship ...
- Remoto
- Híbrido
- Tiempo completo
... clinical trials within pharmaceutical industry, CRO or Collaborative Group, preferably including international or multi-country studies. Experience in oncology clinical trials is strongly preferred. - Desirable previous experience as CRA. - Budget management know how. - Advanced understanding of GCPs and clinical trial legislation. ...
Spain, Barcelona
Ver vacanteFully remote
... I experience - Experience managing CAR-T/ FIH studies Precision's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases ...
€140,000 - €200,000 a year
About the role We are seeking an experienced TAVI Clinical Specialist to play an integral role in supporting the execution of clinical trials while advancing clinical evidence and valve science. The Clinical Specialist will provide procedural and clinical trial case support, contribute to trial enrolment, and identify ongoing ...
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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
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.
... and duties: - Identify, recruit and clinically assess patients eligible for research studies. - Perform study-related clinical evaluations according to Good Clinical Practice (GCP). - Collaborate in the design, development and implementation of investigator-initiated clinical research projects. - Coordinate clinical research ...
Spain, Barcelona
Ver vacantede 50000 a 85000 €/año
... customers, employees, and communities. The Role Veeva Systems is looking for Consultants and Senior Consultants who have some content management expertise and/or, clinical trials expertise and/or software implementation expertise. As a member of our Professional Services team, you will be responsible for understanding our customers’ ...
- Remoto
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Full-time hours
... remotely, with flexibility to be based anywhere in Spain, with preference for Madrid or Barcelona area. As a Global GCP/PV Auditor, you will help ensure that clinical and pharmacovigilance activities are conducted in line with applicable regulations, standards and internal procedures. You will plan and conduct audits, assess ...
- Remoto
- Híbrido
- Presencial
- Contrato
9k / year
En pocas palabras Posición: Clinical Research Associate Localización: Azuqueca de Henares. Contrato: Paternidad- Aprox 1 año. Experiencia: 1 o 2 años de experiencia ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, ...