23.05.2024 | Pełny etat | PrecisionscientiaOf clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well organized, quality regulatory submissions in compliance with applicable regulations. The RM coordinates and prepares regulatory documents for submission
Zobacz później23.05.2024 | Pełny etat | Wrocław | CluePointsCluePoints is an international, innovative, fast-growing (SaaS) company delivering business intelligence for clinical trials and are the premier provider of Risk-Based Quality Management (RBQM) and Data Quality Oversight solutions for Sponsors and CROs, our software products enable both risk
Zobacz później23.05.2024 | Pełny etat | Gdańsk (Gdańsk) | CluePointsWe are a disruptive, leading, and innovative SaaS company developing software and services that revolutionize how clinical trials are managed and new drugs are brought to market. Established in 2012, we have taken the Pharmaceutical industry by storm and are looking for exceptional individuals
Zobacz później23.05.2024 | Pełny etat | Warszawa | CluePointsCluePoints is a disruptive SaaS company developing Our best-in-class AI-driven software products that are revolutionizing how clinical trials are managed and new drugs are brought to market. Since Establishing in 2012, we are spearheading the use of Machine Learning and Advanced Statistical
Zobacz później23.05.2024 | Pełny etat | Parexel InternationalExperience - all types of visits. Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Ability to perform all clinical monitoring activities independently. Strong interpersonal, written, and verbal communication skills within
Zobacz później23.05.2024 | Pełny etat | Warszawa | Precision for MedicineOf clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well organized, quality regulatory submissions in compliance with applicable regulations. The RM coordinates and prepares regulatory documents for submission
Zobacz później23.05.2024 | Pełny etat | Wrocław | SmartBearWant to know more about BitBar You can even have a free trial to check it out
Zobacz później23.05.2024 | Pełny etat | Wrocław | CluePointsWe are a disruptive, leading, and innovative SaaS company developing software and services that revolutionize how clinical trials are managed and new drugs are brought to market. Established in 2012, we have taken the Pharmaceutical industry by storm and are looking for exceptional individuals
Zobacz później23.05.2024 | Pełny etat | Gdańsk (Gdańsk) | CluePointsCluePoints is an international, innovative, fast-growing (SaaS) company delivering business intelligence for clinical trials and are the premier provider of Risk-Based Quality Management (RBQM) and Data Quality Oversight solutions for Sponsors and CROs, our software products enable both risk
Zobacz późniejNie trać już pracy!
Otrzymuj codziennie nowe oferty pracy przez e-mail do Clinical Trial Assistant w Polska.