01.05.2024 | Pełny etat | Warszawa | IQVIA ArgentinaIn a health care or other scientific discipline or educational equivalent Experience in on-site monitoring of clinical trials Alternatively, you should have an equivalent combination of education, training and experience Written and verbal communication skills including good command of Polish and English
Zobacz później01.05.2024 | Pełny etat | Kraków | Ryvu PRMT5Under moderate supervision and makes decisions frequently that have a direct impact on Quality in Ryvu’s Clinical trials. Mentor QA staff Train junior QA team members and
Zobacz później01.05.2024 | Pełny etat | Warszawa | Amgen Inc. IRPrimary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations Maintain the quality and scientific integrity of clinical trials
Zobacz później30.04.2024 | Pełny etat | Alimentiv IncAnd team to provide data management support. Ensure approved study documentation is maintained and properly stored in the trial master files. Manage project resources per budget and within expected timeframes. Develop or assist with the project training development and delivery, for investigators, clinical
Zobacz później30.04.2024 | Pełny etat | AltoidaFor clinical trials, as well as sensitive monitoring of disease progression. Altoida’s mission is to provide life sciences companies with actionable insights using real-world data to increase the success rate for novel therapeutics, and usher in a new era of precision neurology using digital biomarkers. Our
Zobacz później30.04.2024 | Pełny etat | Łódź | Hitachi Vantara CorporationAssessment reporting, corrective action plan alignment with the suppliers and verify the effective closure of corrective action plan items by the supplier side Parts Qualification You lead the production part approval process (PPAP) for the new supplier parts/materials, including the coordination of trial
Zobacz później29.04.2024 | Pełny etat | MedpaceMedpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Poland, particularly in our Warsaw office. Clinical Trial Managers with expertise in Infectious Disease are welcome
Zobacz później29.04.2024 | Pełny etat | Warszawa | IteratoAnd sustainable. Compensation Join us for 32+ hours per week. Compensation for the role depends on your software development skills, and ranges between 12100 - 26000 PLN net monthly (if B2B contract). A trial period may apply. 100% remote work possible. Characteristics Easy-going and inclusive work environment
Zobacz później29.04.2024 | Pełny etat | iDealsOf industries to ensure secure confidential document sharing for online due diligence, fundraising transactions, corporate reporting, licensing, clinical trials, and other business goals. iDeals Board A cloud platform with web and mobile applications used by board members, CEOs, executives, and corporate
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