12.04.2024 | Pełny etat | Warszawa | PostEraPostEra is building a modern 21st-century biopharma. We're using our advances in machine learning to accelerate Medicinal Chemistry and bring more cures to patients. PostEra advances small molecule programs through partnerships with biopharma while also advancing its own internal pipeline. We've rai
Zobacz później23.04.2024 | Pełny etat | Warszawa | Psi CRO AgWill 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 in the database
Zobacz później22.04.2024 | Pełny etat | Warszawa | IQVIA ArgentinaWill be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator. As a pivotal member of the site team, you will be involved with a variety of administrative tasks
Zobacz później19.04.2024 | Pełny etat | Dataprise, LLCThere. What You’ll Do Monitor cyber security tools to identify, triage, and report security incidents to customers. Leverage available cyber security capabilities to contain security incidents to prevent the lateral spread of malware or lateral movement of attackers. Conduct cyber security investigations
Zobacz później19.04.2024 | Pełny etat | Warszawa | Cogent BiosciencesFunctional team members to external consultants, CRO partners, key opinion leaders, investigators, and various committee members to achieve efficient, cost effective, and high-quality design of the clinical development lop an understanding of the clinical and competitive environment and work
Zobacz później18.04.2024 | Pełny etat | Warszawa | ArvinasPresentations to stakeholders, healthcare providers, and patient nd scientific conferences to collect and report relevant scientific and clinical st with Arvinas-sponsored clinical trials and drug development liantly facilitate the submission and review of investigator
Zobacz później18.04.2024 | Pełny etat | Warszawa | ArvinasHealthcare providers, and patient nd scientific conferences to collect and report relevant scientific and clinical st with Arvinas-sponsored clinical trials and drug development liantly facilitate the submission and review of investigator-sponsored research proposalsServe
Zobacz później14.04.2024 | Pełny etat | Warszawa | GlaxoSmithKlineExpertise and will support continuous improvement and the implementation of best practices. Key responsibilities Author and lead the preparation of clinical regulatory documents including, but not limited to protocols, clinical study reports, NDA/MAA CTD submission documents, investigator brochures
Zobacz później13.04.2024 | Pełny etat | Warszawa | Linical Europe• Prepare the submission to the Independent Ethics Committees (central and local) and when applicable to Competent/Regulatory Authorities • Assists in developing of Investigator and Institution contracts and budget template, negotiates budgets with sites and arranges site payments • Participates
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