Clinical Research Jobs in Warsaw

At AbbVie we are committed to advancing innovative medicines and improving patients lives around the world. We are currently looking for a Contract Management Specialist to join our Clinical Operations. In this role you will support clinical research activities and contract management processes for...

PSI is seeking a Medical Monitor (Oncology) to join our international Medical Monitoring team.In this role you will provide medical oversight and expertise across global clinical trials working closely with study sponsors investigators sites project teams and other clinical research professionals. Y...

Assists with set up and maintenance of the Trial Master File (TMF). Serves as main point of contact for all TMF-related activities for assigned projects. Processing and indexing of project documents for the TMF in accordance with project-specific guidelines and relevant SOPs. Upon study closure assi...

The Central Monitoring and Risk Management is at the heart of AbbVies end-to-end RBQM model - a critical pillar required in AbbVies mission to be a world-class R&D organization.The Central Monitor Manager is responsible for managing a cohesive team of front-line central monitor staff to deliver best...

The Project Manager is responsible for the planning management and control projects run by the IT team in the delivery of technology to the Ergomed business and the delivery and hand over of the systems and capabilities into the production systems and business environments within defined and agreed...

The Central Monitoring and Risk Management is at the heart of AbbVies end-to-end RBQM model - a critical pillar required in AbbVies mission to be a world-class R&D organization.The Central Monitor Manager is responsible for managing a cohesive team of front-line central monitor staff to deliver best...

The Director Business and Process Optimization serves as a key member of the leadership team providing strategic leadership in the direction and execution of the operations and resourcing for the department in a complex cross-functional environment to develop and execute strategies that ensure conti...

The Senior Benefit-Risk Associate will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Key responsibilities: Participating in signal detection activities including set-upReviewing line listings required for preparati...

The Director Clinical Vendor Strategy leads Ergomeds clinical outsourcing strategy and vendor governance across the clinical development portfolio. Partnering with Clinical Operations Vendor Management Therapeutic Strategy Regulatory Quality and Finance teams this role drives vendor selection strate...

Responsible to coordinate and develop competitive and flexible strategies for potential awards in oncology and oncology-related indications leveraging expertise operational capabilities and technologies to ensure client needs are addressed in the pre-award activities.Serves as the lead oncology stra...

Collects validates and maintains data from internal and external sources to support feasibility and operational activities.Analyses clinical trial site investigator and operational data to identify trends patterns and opportunities for improvement.Develops and maintains standard reports dashboards a...

Job DescriptionAs Digital Experience Marketing Manager you bring the Ergomed brand to life across three channels: LinkedIn business presentations and our brand websites. Working from the commercial and brand strategy defined by Brand Managers you turn complex ideas and brand messaging into content c...

IMPORTANT: after you apply please check your email. We send you a link to complete your application it is not considered until that last step is done. If you do not see it check your spam folder.This is a fully remote position open to candidates based in Poland.Pay: $100$200/hrRole Title: Bilingual...

Job Overview The Clinical Study Report (CSR) Document Specialist is responsible forthe coordination formatting quality control document management and finalization of Clinical Study Report appendices for assigned studies. This role works closely with TMF Managers Study Leads Medical Writers Biostati...

Position SummaryResponsible for the management of the end-to-end investigator/site payment processes including payment calculations creation and management of purchase orders and clinical trial payments. Acts as liaison among colleagues within Contract & Centralized Services other GCO teams and Site...

The Sr Manager Global Site Activation Legal Liaison is responsible for providing expert operational support and guidance for clinical trial contracting activities when IQVIA Biotech is a contracting party. This role serves as a key point of contact for contracting matters ensuring efficient issue re...

Job Overview:Acts as the primary client lead for complex clinical studies or programs driving operational delivery across multiple vendors and teams. Develops and executes riskmanagement strategies resolves escalated project issues and provides line management and talent development for project mana...

Senior QA EngineerThe RoleWe are seeking an experienced Senior QA Engineer to design develop and maintain automated test suites for ETL pipelines and complex data processing workflows in the healthcare domain (Python PySpark Databricks). You will be responsible for ensuring the quality of platforms...

Providing support to other activities undertaken by the project team on behalf of the client and the companyLine Manages assigned ICSR staffCreates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures trainings and any other actions to increase ICSR...

IQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn...