Medical Management Jobs in Poland

Job DescriptionThe Medical Reviewer II is responsible for medical review of lCSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client.For the Client:To review a More...

For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e More...

Your main responsibilities:Creating longterm carrier management strategies in alignment with the companys business objectivesManaging business relationships with domestic and international carriersNegotiating cooperation terms with courier service providers ensuring favorable financia More...

Your main responsibilitiesManaging relationships with domestic and international carriersNegotiating cooperation terms with carriers ensuring favorable financial and operational conditionsDeveloping and implementing strategies for cost and transportation efficiency optimizationMonitor More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in WarsawResponsibilities:Medical point of contact for internal project team study sites and st More...

The Medical Reviewer I is responsible for medical review of lCSRs and literature review writing of signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. Responsibilities include:To revie More...

Therapeutic area: OncologyTerritorial scope (districts): lskie maopolskie witokrzyskie podkarpackie lubelskie.The Medical Science Liaison (MSL) is a nonpromotional field based scientific expert in a given therapeutic area(s) that strategically supports the medical and scientific objec More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in WarsawResponsibilities:Medical point of contact for internal project team study sites and st More...

Responsibilities include:To review and approve postmarketing 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 Com More...

As a WFM Planner you will join a dynamic Workforce Management team collaborating with 56 other WFM planners to own and deliver capacity plans for your region. You will work closely with a dedicated WFM Analyst and be supported by a Global Planning Lead to ensure datadriven decisionmak More...

Tasks:You will be responsible for modeling internal customers requirement for material master data in SAP S4 systemsYou work closely with our internal customers to gather and discuss material master related business requirementsYou consolidate the requirements derive the technical con More...

International and country level medical engagement projects management (internal and external scientific events HCPs logistics management scientific communication projects).Support and lead defined stages in the defined geographies Medical Programs management: Managed Access (compassi More...

The Senior Manager of Quality Management is responsible for leading one or more teams within Quality Management in line with global strategic objectives. The Senior Manager of Quality Management collaborates with global operational functions to ensure Pharmacovigilance and Medical Inf More...

PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in Polish and English.  Responsibilities  To provide approved responses to med More...

The Quality Management Officer is responsible for ensuring that Quality Events (QEs) and Corrective and Preventative Actions (CAPAs) are completed in accurate and timely fashion and are managed in compliance with global regulations legislation and PrimeVigilance requirements.Lead the More...

Your main responsibilitiesManaging relationships with carriers specializing in the delivery of heavy and oversized productsNegotiating contracts and cooperation terms including additional services such as assembly and installationDeveloping strategies and processes to optimize transpo More...

Key Responsibilities Invoice Processing and Verification: Manage the endtoend process of vendor invoice management including receipt verification and processing of invoices using SAP systems.Automation and System Integration: Utilize SAP ERP integrations automation tools such as More...

The Risk & Compliance team ensures that policies/procedures are in compliance with Polish and European legal regulations regarding risk management and business continuity. They are actively involved in the risk management process within the organization and aid business processes More...

The Risk & Compliance team ensures that policies/procedures are in compliance with Polish and European legal regulations regarding risk management and business continuity. They are actively involved in the risk management process within the organization and aid business processes More...

About This Role:Biogens IT Risk Management (ITRM) function sits within the Cybersecurity organization and leads ITs efforts to identify and mitigate risks to the confidentiality integrity and availability of Biogens systems and data. The IT Risk Manager will report to the Head of IT R More...