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Making Data Science Work for Clinical Reporting

Learn to apply data science principles and tools effectively in clinical trial reporting while maintaining quality and compliance.

Learn to apply data science principles and tools effectively in clinical trial reporting while maintaining quality and compliance.

This comprehensive course demonstrates how to integrate data science methodologies into clinical reporting workflows. Students learn to balance efficient data analysis with regulatory requirements, quality standards, and transparency needs. The curriculum covers version control, reproducible research practices, code reusability, and risk management in clinical trials. Through practical examples and hands-on exercises, participants master the application of modern development practices while ensuring compliance with clinical reporting standards.

Instructors:

English

پښتو, বাংলা, اردو, 2 more

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Making Data Science Work for Clinical Reporting

This course includes

9 Hours

Of Self-paced video lessons

Intermediate Level

Completion Certificate

awarded on course completion

2,699

Audit For Free

What you'll learn

  • Master data science applications in clinical reporting

  • Implement version control and Git workflows effectively

  • Develop robust and reusable code for clinical analysis

  • Understand quality assurance and validation requirements

  • Apply DevOps practices in clinical settings

  • Assess and manage risks in clinical coding

Skills you'll gain

clinical reporting
R programming
Git
version control
agile development
DevOps
data science
clinical trials
reproducible research
InnerSource

This course includes:

289 Minutes PreRecorded video

7 assignments

Access on Mobile, Tablet, Desktop

FullTime access

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There are 7 modules in this course

This course bridges the gap between data science and clinical reporting requirements. Through seven comprehensive modules, students learn to apply data science principles while maintaining compliance with clinical trial standards. The curriculum covers essential topics including version control, code quality, risk management, and reproducible research practices. Students gain practical experience with tools like Git and R, while learning to implement DevOps and agile methodologies in a clinical context.

Making Data Science work for clinical reporting

Module 1 · 54 Minutes to complete

The burden of being faultless and transparent

Module 2 · 1 Hours to complete

Bringing DevOps practices and agile mindset to clinical reporting

Module 3 · 2 Hours to complete

Version control and git flows for reproducible clinical reporting

Module 4 · 1 Hours to complete

Making code reusable and robust in clinical reporting — a call for InnerSourcing

Module 5 · 2 Hours to complete

Assessing and managing risk

Module 6 · 2 Hours to complete

Conclusion

Module 7 · 4 Minutes to complete

Fee Structure

Payment options

Financial Aid

Instructors

Dinakar Kulkarni
Dinakar Kulkarni

1,949 Students

1 Course

Developer Tooling Lead and Clinical Data Science Expert

Dinakar Kulkarni has established himself as a leader in developer tooling and clinical data science at Genentech. As Developer Tooling Lead, he specializes in implementing data science principles in clinical reporting environments. His expertise is demonstrated through his role as instructor for the course "Making Data Science Work for Clinical Reporting," where he teaches intermediate-level concepts combining data science tools with clinical reporting practices. His course covers crucial areas including version control, risk assessment in codebases, and the implementation of data science principles in clinical settings. His work focuses on bridging the gap between traditional clinical reporting and modern data science methodologies, helping professionals understand how to effectively apply tools like R and Python in clinical contexts. His expertise in DevOps practices and agile methodologies contributes to Genentech's mission of advancing healthcare through innovative data science applications.

Kamila Duniec
Kamila Duniec

4.2 rating

6 Reviews

2,396 Students

1 Course

Pharma Biometrics Specialist

Kamila Duniec is a Data Scientist at Genentech with more than fifteen years of experience in pharmaceutical drug development biometrics. Known for an enthusiastic embrace of Agile practices, Kamila has taken on roles as both Scrum Master and Product Owner, in addition to serving as Statistical Programmer and Subject Matter Expert for systems and processes. Their expertise bridges clinical data science and agile methodologies, focusing on optimizing workflows and innovation within biometrics teams. Kamila offers the course “Making Data Science Work for Clinical Reporting,” empowering learners with practical knowledge in data-driven pharmaceutical reporting and Agile teamwork.

Making Data Science Work for Clinical Reporting

This course includes

9 Hours

Of Self-paced video lessons

Intermediate Level

Completion Certificate

awarded on course completion

2,699

Audit For Free

Testimonials

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Frequently asked questions

Below are some of the most commonly asked questions about this course. We aim to provide clear and concise answers to help you better understand the course content, structure, and any other relevant information. If you have any additional questions or if your question is not listed here, please don't hesitate to reach out to our support team for further assistance.