Clinical Data Expert

We're a privately owned company that values its employees and invests in their professional development and success. Our company overview highlights our commitment to quality and excellence.Role ResponsibilitiesThe Clinical Data Scientist will report to the Clinical Data Science Manager and Centralized Monitoring, working with clinical trials patient and...

Site Name: Warsaw, PolandClinical Writer ExpertThe Clinical Writer Expert is responsible for delivering high-quality written content to support the company's mission. This role involves working independently or collaboratively with teams to draft, review, and approve written assignments. The ideal candidate will have a strong understanding of clinical trials...

Job SummaryWe are seeking a skilled Clinical Development Medical Review Expert to join our team. As a key member of the Oncology Clinical Development organization, you will be responsible for ensuring the medical consistency and integrity of clinical data.Main ResponsibilitiesData Review and Interpretation: Responsible for reviewing and interpreting clinical...

As a Clinical Research Expert at TN Poland, you will be responsible for providing expert guidance on regulatory matters and ensuring compliance with complex regulatory issues and projects.Responsibilities:Conduct regulatory intelligence gathering to support development of regulatory roadmaps.Author and maintain documentation to sustain regulatory...

Job DescriptionThis position is a key role in the development and maintenance of data quality standards. The successful candidate will lead the implementation and maintenance of internal data quality control programs, acceptance criteria for data from external sources, and perform related programming tasks.The ideal candidate will collaborate with the...

Clinical Data ManagerAs a Clinical Data Manager at Hays Poland, you will be responsible for leading the planning and execution of data management methodologies for assigned clinical studies.You will collaborate with study teams to implement data management strategies and practices that ensure high-quality data delivery.Key responsibilities include designing...

Your RoleAs a Director, Medical Review Scientist, you will be responsible for performing medical review activities across multiple oncology studies with a wide range of therapeutic modalities and tumor types.Key ResponsibilitiesDevelops a Medical Review Plan (MRP) for the study, which details the scope of the medical review and appropriate timelines s/he...

We are seeking an experienced Clinical Data Science Specialist to join our Clinical Trials team at PSI CRO. As a key member of our team, you will be responsible for developing and implementing data science solutions to support our clinical trials operations.About the RoleDevelop and implement data science solutions to support our clinical trials...

At ICON plc, a world-leading healthcare intelligence and clinical research organization, we're seeking a highly skilled Pharmacovigilance Assistant to join our dynamic team in Warsaw.This role plays a vital part in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials. As a Pharmacovigilance...

As a Data Management and Analysis Expert at PSI CRO, you will be responsible for managing and analyzing complex datasets from multiple sources. You will work closely with our Central Monitoring Manager to develop and implement data management systems that support our clinical trials operations.About the RoleManage complex datasets from multiple sources,...

We are looking for an experienced Clinical Data Specialist Lead to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for providing DM operational input into study design, protocol, and study planning.The ideal candidate will have experience in clinical data management processes, standards, and systems, as...

At PSI CRO, we are dedicated to delivering high-quality services in clinical trials. As a Clinical Trials Data Scientist, you will play a vital role in our team by working with patient and operational data, developing new data solutions, and setting up Risk-based Monitoring systems.About the RoleYou will participate in the selection of the Risk-Based...

technologies-expected : EDC systems responsibilities : Leading the planning and execution of data management methodologies for assigned clinical studies Collaborating with study teams to implement data management strategies and practices that ensure high-quality data delivery Designing and setting up electronic Case Report Forms (eCRFs) and electronic data...

ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development. We're seeking a highly skilled Safety Scientist to join our diverse and dynamic team.As a Safety Scientist at ICON, you'll be responsible for designing and analyzing clinical trials, interpreting complex medical...

About UsWe are a privately owned company that values its employees. Our goal is to provide excellent working conditions and opportunities for personal and professional growth.Job SummaryThe Clinical Data Scientist will play a key role in our team by developing new data solutions, setting up Risk-based Monitoring systems, and managing complex datasets.Develop...

Job DescriptionAt TN Poland, we are seeking a highly skilled Clinical Research Professional to join our international team. As a Senior Clinical Trial Specialist, you will play a crucial role in providing feasibility services, contributing to business development, and ensuring the smooth conduct of newly awarded trials.This is an excellent opportunity for...

We are looking for an experienced Data Strategy and Governance Expert to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for providing DM operational input into study design, protocol, and study planning.The ideal candidate will have experience in clinical data management processes, standards, and...

Role OverviewThe R&D Procurement Manager in Clinical Services will be accountable for a category of outsourced services needed for GSK's clinical trials.This includes negotiating contracts with suppliers that secure favourable terms for procurement of goods and services contracts in line with the agreed business requirements.The successful candidate will...

Job Title:Field Clinical Engineer, ElectrophysiologyLocation: Łodź area, Warsaw, PolandJob Category:OtherEU Work Permit Required:YesThe OpportunityWe are seeking a skilled Field Clinical Engineer to join our Abbott Electrophysiology Division (EP) team in Poland.This fully field-based role requires daily travel across the assigned territory (Łódź...

Clinical Programming RoleWe are looking for an experienced Clinical Programmer to join our team. The ideal candidate will have a strong background in programming in relational database settings using SQL and/or T-SQL or ETL, as well as experience with data reporting tools in a clinical trial setting.The selected candidate will contribute to the development...