30.04.2024 | Pełny etat | Wrocław | IqviaFor the design and implementation of a hybrid cloud strategy including both public cloud (AWS) and on-premises deployments to support distributed software systems that serve an array of scenarios related to clinical trials and other lines of IQVIA’s pharma/tech business. This is a highly collaborative role
Zobacz później30.04.2024 | Pełny etat | Warszawa | KALE RECRUITMENTMust be familiar with Polish accounting standards, knowledge of international/EU accounting standard is a plus; Experience at least 1 year of previous work experience as an accountant, junior accountant or accountant assistant, experience as a chief accountant and experience in EPC-related industries
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 | Warszawa | Prime Vigilance LtdAnd 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 później30.04.2024 | Pełny etat | Jellyfish HRIf you want to learn Japanese technology - Actively towards the type to take a communication 6 Monthly salary 200.000 yen 7 Trial period 3 months same (Yen if not the same) Including fixed overtime a month time. 8 Working hours Ordinary 750 to 1700 Overtime Monthly average 20 ~ 30 hours Overtime pay
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 później30.04.2024 | Pełny etat | Warszawa | Mondelēz International w PolsceFits Sharing the costs of sports activitiesPrivate medical careLife insuranceFlexible working timeRetirement pension planParking space for employeesAnnual bonusMulti-cafeteria MyBenefitsEmployment awardsContract for an indefinite period without a trial period
Zobacz później29.04.2024 | Pełny etat | AppfireTo 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 allowance 200 PLN/month to cover your electricity and internet bills Lunch Card 300 PLN
Zobacz później29.04.2024 | Pełny etat | Warszawa | GlaxoSmithKlineAs mentor and SME for DS&M team Why You? What skills 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
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