Clinical Study Programmer Senior

Senior Clinical ProgrammerLocation: home-based in Eastern EU (Poland, Hungary, Serbia)Why IQVIAData Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading CRO while...

About the Role:The Global Study Manager will be responsible for supporting the delivery of clinical studies within Global Medicines Development (GMD) to time, cost, and quality.This role will involve working cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with the Global Study Associate...

Job TitleClinical Research Associate SMDescriptionThis is an exciting opportunity to join our team as a Clinical Research Associate. The successful candidate will be responsible for performing site monitoring visits, working with sites to adapt and track subject recruitment plans, administering protocol and related study training, and ensuring site documents...

Job SummaryWe are seeking a highly experienced Centralized Monitoring Manager to join our team at PSI CRO.The successful candidate will have strong leadership skills, excellent communication abilities, and experience in clinical study management.Key responsibilities include:Leading and facilitating initial and ongoing study Risk Management...

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...

Global Study Manager - Biopharma (12 months fixed term contract/secondment), WarsawClient:Location: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference: 25231bc49ec4Job Views: 25Posted: 23.01.2025Expiry Date: 09.03.2025Job Description:The Global Study Manager is a member of an extended global study team supporting the delivery of...

Social network you want to login/join with:SAS Programmer in Clinical Trials, WarsawClient:PSI CROLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:8ba4836cfbf6Job Views:3Posted:24.03.2025Expiry Date:08.05.2025Job Description:Actual position's title: Clinical Data ScientistReporting to the Clinical Data Science Manager and...

Social network you want to login/join with:Clinical Study Builder (European Economic Area)At TN Poland, we are seeking a highly skilled Clinical Study Builder to join our team.This role is ideal for individuals who have a passion for medical research and enjoy working in a dynamic environment.The successful candidate will be responsible for designing and...

We are seeking a highly skilled Study Management Coordinator to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for overseeing end-to-end study-related activities and ensuring the delivery of high-quality data management solutions.The ideal candidate will have experience in clinical data management...

About the Job:We are seeking a highly skilled and experienced Global Study Manager to join our team at TN Poland. The successful candidate will be responsible for managing clinical studies from initiation to closure, ensuring timely delivery, within budget and to the required quality standards.Main Responsibilities:To oversee the delivery of clinical studies...

Job OverviewParexel is currently seeking a Clinical Programmer to join our team in various locations across Poland, Czech Republic, Lithuania, Hungary or Serbia.This role will be responsible for providing data review and trial management deliverables across all compounds and trials where these are required.The successful candidate will work closely with...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.Job DescriptionWe are seeking a highly skilled Clinical Research Associate to join our team. The successful candidate will be responsible for performing site monitoring visits, working with sites to adapt and...

We are seeking a highly motivated Global Clinical Operations Coordinator to join our team at TN Poland. As a key contributor to our clinical operations department, you will be responsible for coordinating and supporting logistics for clinical trials.Responsibilities:Coordinate study/site supply management during pre-activation and subsequent course of the...

Job Summary:This Clinical Research Associate position is an excellent opportunity for individuals passionate about clinical research and patient outcomes. As a key member of our team, you will contribute to the success of clinical trials, working closely with study sites, sponsors, and internal stakeholders to ensure seamless project execution.Main...

Key ResponsibilitiesThe Clinical Programmer will be responsible for:Creating external data transfer specifications, ensuring external clinical trial data are compatible with the clinical database to support data integration, analysis and reporting.Planning, set-up, and acquisition of external clinical data at the study level.Liaising with and reviewing work...

Role Overview:The Clinical Research Associate will play a critical role in supporting the execution of clinical trials at study sites. This position requires excellent organizational, communication, and problem-solving skills, with a focus on ensuring high-quality data and compliance with regulations.Main Responsibilities:Site management and monitoring...

Job DescriptionClinical Trial Safety Scientist:  Key Responsibilities  Ensure consistent processes and efficient review of critical clinical/safety data.Review patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency, and generate applicable queries as needed for appropriate medical assessment...

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...

Oncology Clinical Development TeamWe are expanding our Oncology Clinical Development organization and seeking experienced professionals to join our team. As a Director, Medical Review Scientist, you will be responsible for performing medical review activities across multiple oncology studies.Key ResponsibilitiesMedical Review ActivitiesPerform medical review...

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...