Senior Clinical Programmer I

hace 20 horas

Barcelona, España AstraZeneca GmbH A tiempo completo

Job Title: Senior Clinical Programmer I

Career Level - D1

Introduction to role

As a Senior Clinical Programmer I, you will be at the forefront of programming, dashboard development, and validation of data cleaning and review listings for ongoing clinical studies. This role demands high technical skills and industry knowledge to independently perform programming tasks while exercising judgment in complex situations. You will also contribute to cross-functional initiatives with high complexity, driving innovation and excellence in clinical programming.

Accountabilities

  1. Design, develop, implement, and validate complex programs created in SAS/Python/R or dashboard applications such as PowerBI/Spotfire.
  2. Work towards the design, development, implementation, and validation of PowerBI dashboard applications.
  3. Program independently with efficiency and quality to process, analyze, and report clinical trial data ready for review by clinical study teams.
  4. Contribute to design, develop and implement high-complexity projects or initiatives that are part of the clinical programming roadmap.
  5. Define and build vital processes and tools to perform clinical programming activities for both global and study-level analytical solutions.
  6. Develop best practices that enhance quality, efficiency, timelines, and effectiveness within the function.
  7. Provide technical expertise, cross-training, and support as required to ensure the availability and performance of developed reports and dashboards.
  8. Lead all aspects of documentation associated with programming tasks to ensure compliance with standard operating procedures, guidelines, and best practices.
  9. Ensure high quality in own deliverables and quality delivered by other programmers.
  10. Identify and communicate risk within assigned studies and/or projects.
  11. Collaborate with various teams including data management, development operations, clinical, biometrics, and other relevant cross-functional teams supporting clinical trials.
  12. Develop and maintain data visualization tools including requirements gathering, data provisioning, and building dashboards.
  13. Create and maintain a catalog of reports to aid data cleaning and reporting activities.

Essential Skills/Experience

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

Desirable Skills/Experience

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

Ready to make a difference? Apply now

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