Senior Programmer Clinical Trials

Job DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials.Key Responsibilities:Program data review listings, exception reports, QTL/KRIs, metrics reports, and visualizations in a fast-paced environment for clinical trial data review and management...

Brief DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.Essential Functions/ResponsibilitiesProgram simple to complex data review listings, exception reports,...

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...

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...

Job DescriptionWe are seeking a highly experienced Clinical Trials Director to join our team. In this role, you will be responsible for leading the development and implementation of strategies to ensure the quality and integrity of our clinical trials.Key ResponsibilitiesDevelop and lead study team inspection readiness support meetings.Collaborate with QA to...

About the RoleThe Site Manager is responsible for overseeing the day-to-day activities at the site under the direction of the Country Manager. This key role ensures delivery of enrollment goals while maintaining adherence to local regulations and CARE SOPs in all aspects of conducting clinical trials. The ideal candidate will have a strong background in...

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...

Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Role OverviewPrimeVigilance Ltd is seeking a dedicated Medical Case Reviewer to join our team. The successful candidate will be responsible for reviewing individual case safety reports to ensure compliance with regulatory requirements and client expectations.About the Job:Reviewing individual case safety reports from various sources (clinical trials,...

About Our ClientWe are looking for experienced SAS Programmers with at least 4 years of experience in the pharmaceutical industry, especially in clinical trials. If you know SAS and have experience in creating and processing data in the context of SDTM, ADaM, CDISC, TFE standards, we invite you to apply for the position of Statistical Programmer (SDTM,...

About the RoleWe are seeking a highly skilled Senior Project Manager to lead our clinical trials in Poland. As a key member of our team, you will be responsible for ensuring the successful delivery of projects from start-up to closure.ResponsibilitiesServe as primary contact for sponsors and ensure timely updates on trial progressOversee project planning,...

Job SummaryWe are seeking a highly experienced Senior Clinical Operations Specialist to join our team. In this role, you will be responsible for providing quality management support to study teams and ensuring the integrity of our clinical trials.Key ResponsibilitiesDevelop and maintain guidance and processes to facilitate DOQ support of Study Teams.Provide...

About the Ideal CandidateWe are seeking a highly experienced professional with at least 15 years of industry experience and a minimum of 5 years at a CRO. The ideal candidate will have a strong background in clinical project management, including management of all phases of clinical trials from start-up to closure.The ideal candidate will also have...

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...

Job Title: Clinical Research AssociateAbout the Role:We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team at IQVIA Argentina. As a CRA, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and sponsor expectations.Key Responsibilities:Perform site...

About the RoleAs a Statistical Programmer at Rho, Inc., you will play a critical role in designing and implementing statistical analysis plans for clinical trials. You will work closely with cross-functional teams to develop and maintain software programs, ensuring data accuracy and integrity.The ideal candidate will have strong programming skills in SAS and...

About the RoleThis position is a critical component of GSK's growing oncology antibody drug conjugate (ADC) portfolio. As a Medical Director of Oncology Clinical Development, you will be responsible for leading clinical research activities, developing and executing phase 1-3 interventional clinical trials, and collaborating with medical experts to ensure...

Job SummaryClinical Solutions Group, an IQVIA business, is seeking an SDTM SME for a remote position. The successful candidate will have strong knowledge on SDTM and ADaM specifications. Incumbent must have the ability to follow processes, but not blindly accept policy, while working on a team with strong ADaM experience.Primary Job responsibilitiesDrives...

Career Advancement OpportunitiesThis role offers an exciting opportunity to work with a dynamic team and contribute to the success of our clients.The successful candidate will have a strong understanding of clinical data management and statistical programming processes and standards.Key Responsibilities:Lead the implementation and maintenance of internal...

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job...