Średnia wypłata: zł23 334 /miesięczne
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- ...responsible for authoring comprehensive Statistical Analysis Plans and executing regulatory-grade programming necessary for Analytical and Clinical Validation. You will work remotely, collaborating with cross-functional teams to ensure compliance with FDA and EMA standards. If...KlinicznyPraca zdalna
Sii Sp. z o.o.
Warszawa17 dni temu - ...join our team and help shape and deliver digital health solutions that support oncology care teams in making timely and personalized clinical decisions. Your deep understanding of oncology care delivery will be crucial in translating clinical needs into actionable...KlinicznyPraca zdalna
Sii Sp. z o.o.
Warszawa7 dni temu 130 - 150 zł / stawka godzinowa
...Mile widziane, Jira, Confluence O projekcie, Poszukujemy osoby na stanowisko IT Product Owner (m/k) do obszaru Digital Health / Clinical Systems. Praca jest dedykowana dla międzynarodowej firmy z branży farmaceutycznej. Osoba na tym stanowisku będzie odpowiedzialna...KlinicznyPraca zdalnaITP IT PERFORMANCE sp. z o.o.
Warszawa12 dni temu13300 - 22080 zł
...act as a trusted partner to life sciences organizations, from emerging biotechs to top global pharma., , Focusing on either Veeva Clinical Operations or Veeva Regulatory, you will lead the continuous evolution of our customers' cloud platforms. Instead of just responding...KlinicznyPełny etatUmowa o pracęPraca z domuPraca zdalnaHome officeVEEVA SYSTEMS POLAND sp. z o.o.
Warszawa17 dni temu115 zł / stawka godzinowa
...vitro diagnostic solutions, laboratory automation, advanced systems, and testing technologies that support faster and more accurate clinical decisions., , This is a business-oriented program management role rather than an IT position. Within Global Customer Support, you...KlinicznyPraca zdalnaWINGED IT SP Z O O
Warszawa10 dni temu- ...Clinical Trial Associate position supporting sponsor-dedicated clinical research operations. The role involves coordinating trial administration, managing documentation, and collaborating across teams to ensure regulatory compliance and successful trial execution in a...KlinicznyPodróże służbowe
- ZAKRES OBOWIĄZKÓW: ~ prowadzenie pogłębionej diagnozy psychologicznej i klinicznej (dzieci i młodzież) , ~ prowadzenie konsultacji oraz porad psychologicznych z uwzględnieniem indywidualnych potrzeb i stanu klinicznego pacjentów, ~ opracowywanie opinii psychologicznych...KlinicznyUmowa zlecenieNiepełny etatElastyczne godziny
Mind Health – Centrum Zdrowia Psychicznego- medicover
Warszawa6 dni temu - ...ICON Strategic Solutions seeks a Grants Specialist to manage grant applications and identify funding opportunities supporting clinical programmes. The role involves researching opportunities, developing proposals, ensuring compliance, and tracking grant outcomes within...Kliniczny
- ...strategic roadmap development with hands-on oversight of advanced analytics, AI applications, and decision-support products across the clinical development portfolio. Responsibilities Own and sequence capability-area roadmaps across advanced analytics, automation, and...Kliniczny
- ...A Clinical Trial Associate position focused on payments administration and documentation management within clinical trial operations. The role involves coordinating study materials, maintaining trial master files, managing site access and payments reconciliation, and...Kliniczny
- ...building relationships with key opinion leaders, conducting scientific dialogue on marketed and pipeline products, and supporting clinical research initiatives while maintaining compliance with regulations. Responsibilities Identify and establish professional relationships...Kliniczny
- ...Medical Admin Assistant position supporting clinical trial operations across Eastern European locations. Provides administrative and executive support to medical teams, managing documentation, scheduling, and regulatory coordination to facilitate clinical research activities...KlinicznyPodróże służbowe
- ...Requirements Bachelor's degree in scientific or healthcare-related discipline Pharmacovigilance, drug safety, or related experience in clinical/pharmaceutical setting Strong analytical skills with meticulous attention to detail Excellent communication and...KlinicznyPodróże służbowe
- ...Regulatory Affairs Manager role within Respiratory and Immunology therapy area, leading clinical trial submissions and regulatory strategies across multiple regions. The position involves managing CTA/IND submissions through approval, coordinating cross-functional teams...Kliniczny
- ...Site Activation Partner I facilitates the initiation of clinical trials at ICON Strategic Solutions, ensuring regulatory compliance and supporting study start-up activities. The role involves preparing regulatory documentation, coordinating approvals, and collaborating...KlinicznyPodróże służbowe
168100 - 312100 zł / rocznie
...for quality issues and audit responses. Reports to quality leadership and oversees CAPA team activities, ensuring compliance with clinical trial regulations and guidelines. Responsibilities Lead and mentor CAPA management team members on compliance and quality improvement...Kliniczny- ...Director leading country operations and disease area strategy for Alexion's rare disease portfolio in Poland. The role bridges global clinical development initiatives with local operational delivery, overseeing feasibility planning, trial conduct, and cross-functional...Kliniczny
- ...organizations Practical understanding of learning and development approaches Proven experience building targeted interventions to build and maintain capability Knowledge of supply chain management or manufacturing Knowledge of clinical study delivery (desired)...KlinicznyPraca hybrydowa
- ...ICON seeks a Global Clinical Integration Lead to manage project and programme delivery across multiple European locations. The role focuses on coordinating cross-functional teams, developing project plans, monitoring progress, and engaging stakeholders to ensure successful...KlinicznyPodróże służbowe
- ...and Senior Project Managers based in the EU with strong respiratory therapeutic expertise to lead complex global Phase II and III clinical trials. The role demands proficiency in multi-country trial management, ICH-GCP compliance, and cross-functional team leadership within...Kliniczny
- ...regional business objectives across Western Europe and Advanced Surgery Lead development of sales representative, sales leader, and clinical specialist training programs in partnership with global centers of excellence Oversee new hire onboarding, certification...Kliniczny
- ...Medical Operations Associate to provide senior-level operational support for medical monitoring and drug development projects across clinical research initiatives. The role involves cross-functional coordination, staff mentoring, quality oversight, and process improvement...Kliniczny
- ...ICON seeks a Project Manager for Feasibility & Site Activation to lead global clinical trial start-up strategies across multiple European countries. The role involves overseeing regulatory approvals, site contracts, and study activation timelines while coordinating cross...Kliniczny
- ...Fortrea seeks a Site Budgeting & Contracting Specialist in Warsaw to prepare, negotiate, and manage site agreements and contracts for clinical studies. The role involves maintaining contract tracking systems, ensuring regulatory compliance, and coordinating with internal...Kliniczny
- ...conducting literature searches Administer SharePoint Online and electronic document systems for assigned product portfolios Execute clinical safety program activities including protocol tracking and health authority query management Mentor Pharmacovigilance Associate...Kliniczny
- ...pharmaceutical products to primary care physicians and retail pharmacists. The role involves developing territory strategy, conducting clinical education, maintaining healthcare provider relationships, and ensuring compliance with company standards. Responsibilities...Kliniczny
205850 - 249445 zł / rocznie
...Responsibilities Coordinate and author regulatory documents including IB, safety reports, and clinical study reports Integrate scientific, medical, and regulatory input from cross-functional development team members Use AI-enhanced document development tools...Kliniczny- ...engagement plans and build relationships with advocacy groups and medical organizations Requirements University degree in science or clinical qualification with relevant experience Demonstrated ability to discuss scientific content with diverse audiences Familiarity...KlinicznyPodróże służbowe
- ...Ergomed seeks an EDC Developer to design and build electronic data capture systems for clinical trials using Medidata RAVE and Zelta v1.0. The role involves creating system structures, workflows, edit checks, documentation, and managing post-launch updates under the Data...Kliniczny
105900 - 374100 zł / rocznie
...This role manages the operational and strategic aspects of clinical trial submissions in Poland, guiding projects from strategy development through regulatory approval. Key responsibilities include coordinating submission processes via CTIS portal, conducting quality...Kliniczny
