26.04.2024 | Pełny etat | Johnson & JohnsonClinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols. A Senior Clinical Research Associate may contribute to process improvement, training and mentoring of other Site Managers. 1. Acts as primary
Zobacz później26.04.2024 | Pełny etat | KnewinAffairs Specialist Job Description Summary The Abramson Cancer Center (ACC) of the University of Pennsylvania is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of cancer. The ACC Clinical Research Unit (CRU) is instrumental
Zobacz później26.04.2024 | Pełny etat | Profound ResearchKey to successful execution of clinical trials. Responsibilities · Oversight and management of contracting processes, timing, and outcomes in partnership with appropriate legal counsel · Establish, measure, and report out on contracting status and performance against KPIs · Track and report activity
Zobacz później25.04.2024 | Pełny etat | Wrocław | 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 później25.04.2024 | Pełny etat | Gdańsk (Gdańsk) | 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 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 później25.04.2024 | Pełny etat | Warszawa | AstraZenecatrials and of studies that further characterize the overall benefit and risk and value of products in respiratory therapeutic area (TA) in late stage development. In this role the scientist will seek input from the appropriate functional experts and will coordinate these activities in support of clinical
Zobacz później25.04.2024 | Pełny etat | Warszawa | AstraZenecaNext. Supportive team players, we draw on diverse knowledge from across the business and external partners to come to bear on the toughest medical challenges. Introduction to Role Join us in our mission to eliminate cancer as a cause of death. As a Global Clinical Operations Program Director (GPD
Zobacz później25.04.2024 | Pełny etat | Rzeszów | 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
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