Dobivajte nove poslove putem e-pošte
- ...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright... ...and working practices. Process, review, and resolve rejected Trial Master File (TMF) documents, for complex studies or Sponsor portfolio...Rad od kuće
- ...world-leading healthcare intelligence and clinical research organization. We’re proud to... ...role in designing and analyzing clinical trials, interpreting complex medical data, and contributing... ..., and patient safety throughout the trial process. ~ Collaborating with...
- ...review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding, seriousness assessment, Company causality and comment, listedness...
- ...About ARTIDIS ARTIDIS AG is a clinical-stage health-tech start-up company founded in Basel, Switzerland that has developed the first... ...requirements. Maintain accurate and complete documentation of the Trial Master File globally and conduct site audits, including source...
- ...faster, easier, and more accurate to assess cognition across clinical trials, healthcare settings, and everyday life. Our digital cognitive... ...mindset. Whether we’re supporting a multinational Alzheimer’s trial or developing tools to bring cognitive testing into routine...
- ...services with full accountability. If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to...