19.05.2024 | Pełny etat | Warszawa | Parexel InternationalDemonstrated knowledge of site intelligence at country/cluster level in support of site recommendation - Demonstrated knowledge of clinical trial methodology and the drug development process, related to monitoring clinical trials, GCP, Food and Drug Administration (FDA), or country-specific regulatory
Zobacz później16.05.2024 | Pełny etat | Warszawa | OptimapharmIn statistical methods and nstrate a comprehensive understanding of biostatistical methodologies and stay familiar with regulatory requirements in design, analysis and reporting of clinical joining our fast-growing and prosperous team, you will have an excellent opportunity for further
Zobacz później09.05.2024 | Pełny etat | Warszawa | Novo Nordisk A/SAre you a dedicated clinical trial professional with solid site management experience? Are you highly motivated by being able to make a difference to improving patients’ lives? If yes, keep reading - this role might be just for you! The position As Clinical Research Associate your role is to verify
Zobacz później03.05.2024 | Pełny etat | Warszawa | PSI CRO AGYou will Provide support to startup teams for selected projects Coordinate review and negotiation of clinical trial agreements and investigator grants between PSI staff and study site Perform administrative activities (documents collection/distribution, filing clinical trial agreements
Zobacz później03.05.2024 | Pełny etat | Warszawa | ITP S.AFinancial data to ensure the accuracy of bookings Prepare balance sheet account reconciliations on a monthly basis Execute monthly financial closing process in a timely manner and ensure compliance with accounting policies Maintain accuracy and completeness of trial balances Monthly/quarterly/annual
Zobacz później02.05.2024 | Pełny etat | Warszawa | BMW GroupAccountability, problem solving attitude and hands-on mentality, Ability to present legal information to a diverse audience, Profound knowledge of MS Office tools, Polish and English (negotiation level). What we offer Contract of employment, Flexible working time, Hybrid working opportunities (after trial
Zobacz później01.05.2024 | 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 później25.04.2024 | Pełny etat | Warszawa | BBSTEM Ltd.And expertise you will bring to the role Relevant education degree from Scientific Discipline (Biomedical or Computer) Min. 5 years of data management/clinical trials experience in Pharma, CRO and/or ARO Knowledge of the principles of quality, safety, risk management and compliance (ICH and GCP) Fluent English
Zobacz później24.04.2024 | Pełny etat | Warszawa | IQVIA ArgentinaSenior Site Activation Coordinator (Contract Negotiator) Country Site Activation Join us on our exciting journey! IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective
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