Senior Clinical Programmer

hace 3 días

Barcelona, España AstraZeneca GmbH A tiempo completo

**Job Title - Senior Clinical Programmer**

**Career Level - D**

**Introduction to role**

Are you ready to take on a pivotal role in transforming clinical trials through innovative programming and data visualization? As a Senior Clinical Programmer I, you will be at the forefront of developing and validating complex programs and dashboards for ongoing clinical studies. Your expertise will drive high-quality data analysis and reporting, contributing to cross-functional initiatives with significant impact. This role demands advanced technical skills and industry knowledge, empowering you to independently tackle programming tasks while seeking guidance in complex situations.

**Accountabilities**
- Process, analyze, and report clinical trial data for review by clinical study teams.
- Lead high-complexity projects or initiatives within the clinical programming roadmap.
- Define and build essential processes and tools for global and study-level analytical solutions.
- Develop best practices to enhance quality, efficiency, timelines, and effectiveness within the function.
- Provide technical expertise, cross-training, and support to ensure the performance of developed reports and dashboards.
- Oversee documentation associated with programming tasks to ensure compliance with standard operating procedures, guidelines, and best practices.
- Ensure high-quality deliverables from self and other programmers.
- Identify and communicate risks within assigned studies or projects.
- Collaborate with various teams including data management, development operations, clinical, biometrics, and other relevant cross-functional teams.
- Develop and maintain data visualization tools, including requirements gathering, data provisioning, and building dashboards.
- Create and maintain a catalogue of reports to aid data cleaning and reporting activities.

**Essential Skills/Experience**
- Bachelor’s/Master’s degree or equivalent in computer science, life science or statistics.
- Accomplished programming skills in SAS/Python/R/SQL/Power BI/SpotFire or other dashboard technologies.
- Intermediate knowledge of clinical development process.
- Good knowledge of industry standards.
- Ability to influence relevant stakeholders.
- Excellent analytical and critical thinking skills, writing, communication skills, and ability to work within a cross-functional team.
- Ability to work in a global team environment.
- Technical expertise with data capture, data models, data mining, and visualization techniques.
- Prior experience and understanding of EDC systems like Medidata Rave / Inform / Veeva and Data Platforms like Saama/Entimice, SAS LSAF etc.

**Desirable Skills/Experience**
- Excellent collaborative skills and the ability to manage complexity and change in a dynamic environment.
- Broad knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processes.
- Experience in producing analytical dashboards with Power BI, Spotfire or other Business Intelligence tools.
- Knowledge on MicroStrategy.

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