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Keywords: Worldwide Clinical Trials, Location: Warszawa, Mazowieckie

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Principal Clinical Programmer

: Leads a team of Programmers within Clinical Data Integration and Standards. Drives the development of programming standards... filing of clinical data as well as archiving. Collaborates in the generation of an eCRF global library to ensure...

Company: IQVIA
Posted Date: 14 Jan 2025

Senior Clinical Programmer (SDTM/SAS)

, and implementation of relevant listings and reports to ensure that adequate data quality will be achieved for clinical trials... standard format (SDTM, ADaM), and data from external sources as they have been collected in clinical trials (eg, IxRS systems...

Company: IQVIA
Posted Date: 14 Jan 2025

Associate, Site Contracts - Warsaw - Office Based

, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global... Worldwide Legal Department, study teams, Sponsors, investigators, and/or clinical sites. What you will do Prepare country...

Posted Date: 01 Mar 2025

Senior Medical Writer

Good understanding of common statistical methods used in clinical trials and/or interpretation of their results. Req.... Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP...

Company: IQVIA
Posted Date: 02 Mar 2025

Manager Flexible Resourcing, Sponsor Dedicated in Poland

with one key client in Poland. In our Clinical Functional Service Partnership team, we work in a close partnership with our key... customers to deliver a comprehensive clinical trial management. Within this role, you will manage a team of CRAs/SrCRAs...

Company: IQVIA
Posted Date: 21 Feb 2025

Principal Statistical Programmer

of clinical trials via exploratory analyses of available data, o replicate CRO and CSL statistician analyses for QC Position... programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main...

Company: IQVIA
Posted Date: 14 Jan 2025

Senior Statistical Programmer

planning and reporting of clinical trials via exploratory analyses of available data, Position Qualifications and Experience... and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data...

Company: IQVIA
Posted Date: 13 Jan 2025

Contract Negotiator FSP - Poland

, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials.... Qualifications Bachelor's Degree Related field 5 year relevant sponsor or clinical research organization clinical site contracting...

Company: IQVIA
Posted Date: 10 Jan 2025

Principle Statistical Programmer - Homebased - Eastern Europe

Senior Manager, Clinical Data Integration and Standards, is a key leadership position responsible for providing functional... leadership and managerial oversight for a group of Clinical Programmers who are responsible for programming and standard datasets...

Company: IQVIA
Posted Date: 09 Jan 2025

Digital Engagement Lead

Digital Strategy, focusing on enhancing the end-to-end patient access and engagement experience for clinical trials. This role...’s vision to transform site/patient access and engagement in clinical trials. Define an integrated patient and site journey...

Company: IQVIA
Posted Date: 09 Jan 2025