Description Freelance / Contractual, CRA with experience in Dermatology, Spain The Contractual Clinical Research Associate (cCRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported
Clinical Research Associate IQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in
The Academic Research Organisation (ARO) Platform provides comprehensive sponsor support for the management of clinical trials and studies, covering all phases of research—from Phase I to Phase IV—throughout the entire study lifecycle. The Vall d’Hebron Research
Location: Barcelona - Spain (3 days working from the office and 2 days working from home) This is what you will do: The Associate Director, Global Health Economics & Outcomes Research (GHEOR) Analytics, develops and implements HEOR
Site Contracts Analyst IQVIA Biotech Bulgaria, Serbia, Spain, Slovakia - Homebased IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and
Location: Barcelona - Spain (3 days working from the office and 2 days working from home) This is what you will do: The Associate Director, Global Health Economics & Outcomes Research (GHEOR) Analytics, develops and implements HEOR
Career CategoryClinical Job Description What you will do In this role, the Clinical Scientist Associate Director supports the design, execution, and oversight of clinical trials and other late-phase global clinical studies. The role contributes to protocol development,
Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Are you ready to make a significant impact in the world of oncology diagnostics? As the Associate Director, Diagnostic Partnerships within
Role Barcelona onsite 3 days office/2 days home Would you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment?
Overview and Summary We are Automotive Business Scientists. We empower our clients to turn overwhelming industry data into discovery, action and measured success. We are unique market leaders because we find and examine possibilities through the
Job Description SummaryThe Associate Director, Field Medical Execution is a strategic, execution-focused role within IMACE, reporting to the Director, Field Medical Execution and is accountable for enabling high quality, data driven field medical execution across countries for
Job Description SummaryThe Associate Director, Field Medical Execution is a strategic, execution-focused role within IMACE, reporting to the Director, Field Medical Execution and is accountable for enabling high quality, data driven field medical execution across countries for
The Academic Research Organisation (ARO) Platform provides comprehensive sponsor support for the management of clinical trials and studies, covering all phases of research—from Phase I to Phase IV—throughout the entire study lifecycle. VHIR offers a vacant
Associate Consultant Drug Safety Location: Hybrid - Madrid Type: Full-time The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offersknowledge&tailored (software) solutionsin development, clinical, regulatory & compliance, production and distribution for companies
Join IQVIA and work at the intersection of clinical strategy, data insights and client engagement. This role sits within our planning and strategic services team and focuses on turning data into clear, compelling recommendations that help
Job Overview The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project
IQVIA Biotech is hiring Clinical Research Associate in Spain! IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise
Role Barcelona onsite The Trial Safety Review Center (TRISARC) is a department in the Research and Development function of AstraZeneca. The primary remit of TRISARC is to review large amounts of medical (mainly safety) data flowing
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate! – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs,