Associate Director, Statistical Programming

Director, Statistical Programming Hybrid work, Warsaw Are you an experienced Statistical Programmer with good knowledge of clinical drug development and leadership? Would you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment? Join us at...

Statistical Programming Associate Director, Late Stage Respiratory & Immunology Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology) Would you like to lead clinical studies,...

Statistical Programming Associate Director, Late Stage Respiratory & Immunology Location : Warsaw (PL) Salary: Competitive, with excellent benefits. Hybrid model of work : 3 days in office, 2 days remote per week Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology) Would you like to lead clinical studies,...

Senior Statistical Programmer, Patient Center Solutions Location : Slovakia, Greece, Bulgaria, Estonia, Portugal, Spain, Poland & Serbia. Work Model : Hybrid or Office based The role: Manage a team of Statistical Programming (SP) staff, including hiring, training, and supervising department members. Develop, recommend, and implement standard...

Senior Statistical Programmer, Patient Center Solutions Location : Slovakia, Greece, Bulgaria, Estonia, Portugal, Spain, Poland & Serbia. Work Model : Hybrid or Office based The role: Manage a team of Statistical Programming (SP) staff, including hiring, training, and supervising department members. Develop, recommend, and implement standard...

The Associate Director Standards Developer is primarily responsible for leading the technical development, management and maintenance of AZ end-to-end Clinical Analysis & Reporting Standards activities in their area of expertise ( clinical coding, clinical dictionaries, and data analysis & reporting standards (SDTM, ADaM, TLFs)) with quality and timeliness,...

The Associate Director Standards Developer is primarily responsible for leading the technical development, management and maintenance of AZ end-to-end Clinical Analysis & Reporting Standards activities in their area of expertise ( clinical coding, clinical dictionaries, and data analysis & reporting standards (SDTM, ADaM, TLFs)) with quality and timeliness,...

Location: Warsaw, Poland Play a critical role in making our pipeline accessible to patients. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s...

Location: Warsaw, Poland Play a critical role in making our pipeline accessible to patients. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s...

Are you a Statistical Programmer eager to apply your knowledge and skills in a truly significant setting? Would you like to be a part of a programming group that has direct strategic impact on drug development, playing a key role in getting medicines to patients? Join us today to se what science can do. Typical Accountabilities Working experience in...

Are you a Statistical Programmer eager to apply your knowledge and skills in a truly significant setting? Would you like to be a part of a programming group that has direct strategic impact on drug development, playing a key role in getting medicines to patients? Join us today to se what science can do. Typical Accountabilities Working experience in...

Job Description : Provide line and functional management of Data Management technical experts, with a team size of around 15-20 people. Manage and prioritize resource assignments, as well as workload management across Technical Design and SAS Programming teams ensuring project milestones are met according to agreed timelines with high quality.  ...

Job Description : Provide line and functional management of Data Management technical experts, with a team size of around 15-20 people. Manage and prioritize resource assignments, as well as workload management across Technical Design and SAS Programming teams ensuring project milestones are met according to agreed timelines with high quality.  ...

Join us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability. IQVIA Biostatistics helps...

Statistical Analyst in the Data Quality Management Department Responsibilities: Determining quality control methods for current reports, developing a data quality management system Finding and clarifying quality problems Preparing automatic reporting mechanisms using MS SQL Server (and possibly other programming tools) Preparing reports and...

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based): ...

The Associate Director, Open-Source Developer, is responsible for ensuring the high-quality, timely, and efficient development of open-source infrastructure for clinical programming and effective information management. This pivotal role demands profound experience in Python, R, and SAS programming, coupled with excellent industry knowledge of creating...

Job Overview: As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies. This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum...

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based): ...

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based): ...