11.04.2024 | 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 później11.04.2024 | Pełny etat | KnewinThe execution of the clinical development plan. For assigned programs, be accountable for the study design of clinical trials in Early Development, leading on the preparation of clinical study synopses and being a major contributor to the writing of protocols/major amendments, the design of data collection
Zobacz później11.04.2024 | Pełny etat | RegenxbioWe aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities. The Opportunity The Clinical Delivery Project Manager reports to the Executive Director, Delivery Training and assists
Zobacz później11.04.2024 | Pełny etat | Frends Technology OyThe role from our blog. ???? What do we offer? Competitive salary adequate to your expertise Flexible employer who is willing to adjust the best working methods to your lifestyle Flexible working hours, part-time employment possible, remote work without restrictions - after the trial period. Flat
Zobacz później11.04.2024 | Pełny etat | Wrocław | N-iXPlanning and operational risk monitoring and utilize advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution. We are seeking outstanding candidates with strong project management skills and a passion for delivery excellence, to help drive
Zobacz później11.04.2024 | Pełny etat | Warszawa | AstraZenecaOf late stage product development. This includes but is not limited to the design, delivery, and interpretation of pivotal clinical trials and of studies that further characterize the overall benefit and risk and value of Respiratory and Immunology products in late stage development. This role ensures
Zobacz później11.04.2024 | Pełny etat | Warszawa | IQVIA ArgentinaFor the translation and co-ordination of translations for documents required for submission. Responsible for liaising with local CRA/CTM, Contract Specialist, and Regulatory Lead to enable a rapid clinical trial start up. Work with legal team members and SSU Manager to secure authorization of contracts. Inform team
Zobacz później11.04.2024 | Pełny etat | IQVIA ArgentinaAppreciated. Typical Activities Consultation and collaboration with software development teams Actively participate in Agile practices Assist with infosec assessments Work with cloud infrastructure providers Configure deployment automation frameworks Establishbest practices for consistency among software
Zobacz później11.04.2024 | Pełny etat | Łódź | 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
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