Search current Remoto clinical research study coordinator jobs, vacancies, and employment in España on Jobeax. 1,102 Remoto clinical research study coordinator jobs in España.
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Fully remote
... in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management. Precision for Medicine is looking for Clinical Research Associates II based in Madrid or Barcelona to join our team in Spain. About you - You are calm, thoughtful, and responsive when things don't go as ...
Spain
... clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Responsibilities You will: - Support the preparation and execution of Clinical Investigations and Performance Studies - Assist in developing study documentation (protocols, CRFs, ICFs) - Collaborate with study sites and internal teams ...
Spain, Vitoria
... clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Responsibilities You will: - Support the preparation and execution of Clinical Investigations and Performance Studies - Assist in developing study documentation (protocols, CRFs, ICFs) - Collaborate with study sites and internal teams ...
Spain, Castro
SOLTI #cancerresearch
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
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, ...
Spain
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, ...
Spain
... 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 activities with study coordinators and research nurses. - Contribute to protocol development, ethics submissions ...
Spain, Barcelona
... data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature reviews, background research, and documentation preparation - Assist in drafting components of clinical evidence documentation under supervision - Help coordinate project activities, timelines, ...
Spain, Pamplona
... data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature reviews, background research, and documentation preparation - Assist in drafting components of clinical evidence documentation under supervision - Help coordinate project activities, timelines, ...
Spain, Coruña
... data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature reviews, background research, and documentation preparation - Assist in drafting components of clinical evidence documentation under supervision - Help coordinate project activities, timelines, ...
Spain, Málaga
... data‑related tasks - Contribute to scientific and medical writing, including study summaries and evidence-based content - Support literature reviews, background research, and documentation preparation - Assist in drafting components of clinical evidence documentation under supervision - Help coordinate project activities, timelines, ...
Spain, Alacante
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 ...
Spain
Fully remote
... within Clinical Operations position within a CRO, and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation. - Experience managing studies within Oncology - Working understanding of GCP/ICH guidelines and the clinical development process - Ability ...
Spain
Fully remote
... within Clinical Operations position within a CRO, and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation. - Experience managing studies within Oncology - Working understanding of GCP/ICH guidelines and the clinical development process - Ability ...
Spain
... experience in clinical research, study start-up, regulatory affairs, or a related scientific environment, including international experience. - Strong knowledge of clinical trial regulations, GCP, ICH guidelines, and the drug development process. - Proven experience managing complex, multi-country clinical trial start-up activities. ...
Spain
Full-time hours
... clinical and medical experience and knowledge in the area of clinical research, and safety to direct risk management activities, and serves as an advisor to Clinical Affairs to support publications, abstracts and presentation of clinical research. Ensures critical input to establish and implement required product safety ...
Spain
Fully remote
... organization." - Hands-on experience as medical monitor in oncology clinical trials, including review of emerging safety data and medically based decision-making during study conduct. - Member of safety data review boards in clinical trials, or equivalent experience. - Understanding of Good Clinical Practice regulations, International ...
Spain
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. ...
Spain
Full-time hours
... essential. - Applications from candidates with pharma experience may also be considered. - Familiarity with standard business and eClinical systems used in Clinical Research is desirable. - ICH and GCP regulations in relevant geographies. - Solid clinical knowledge and understanding of clinical research and protocol design. ...
Spain
€140,000 - €200,000 a year
... demonstrating competency in CT and echocardiographic imaging, applicable clinical study documentation and Instructions for Use, procedural best practices, clinical evidence, approved product messaging and the competitive landscape. - Interface with clinical trial sites, demonstrating expertise in all technical aspects ...
Spain