24.04.2024 | Pełny etat | Warszawa | IQVIA LLCassistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures
Zobacz później24.04.2024 | Pełny etat | Gdynia | AppfireOff, regardless of years of experience Wellness Days additional time off each month to recharge and take care of yourself Indefinite Employment Contract from day one, no trial periods MyBenefit Platform 150 PLN/month to spend on Multisport card or available shops, restaurants, gyms, etc. Home Office
Zobacz później23.04.2024 | Pełny etat | Radom | EvidoseAssociated with these products, despite the promises made. At Evidose, we are committed to cutting through the noise. By leveraging decentralized trials, advanced technology, and user-centered design, we aim to set the gold standard for data-driven insights, bringing clarity and rigor across all wellness
Zobacz później23.04.2024 | Pełny etat | Katowice | Thermo Fisher Scientific Inc.In clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future. Do you have a data
Zobacz później22.04.2024 | Pełny etat | Warszawa | IQVIA ArgentinaEnvironment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Zobacz później22.04.2024 | Pełny etat | Warszawa | Ergomed GroupAnd approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding, assessment of seriousness, listedness/expectedness and Company causality, as well as writing of Company comment
Zobacz później22.04.2024 | Pełny etat | Precision Medicine Group, LLC.Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures - Work Instructions (SOPs/WIs); regulatory directives study specific
Zobacz później22.04.2024 | Pełny etat | PrecisionscientiaHungary, Romania, Poland, Slovakia, Serbia, Spain and UK. Position Summary The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct
Zobacz później22.04.2024 | Pełny etat | Łódź | Infosys Poland Sp. z o.o.With external customers Maintaining and reconcile AR accounts Collaboration with client, customers other departments We offer to the candidates Great atmosphere Internal trainings No trial period Career in the multinational company Set of social benefits to choose from #J-18808-Ljbffr
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