This specialization is designed for individuals and teams that will be running or interacting with clinical trials. In four courses, learners will develop insights and build the skills they need to design, manage, and monitor clinical trials as well as analyze, document, and communicate the results. Learners will also learn best practices regarding ethics, safety, participant recruitment, regulatory compliance, and reporting standards. The core principles and skills of the specialization will lay the foundation for a successful career in the field.

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Clinical Trials Operations Specialization
Design and Conduct Successful Clinical Trials. Build skills for conducting successful and impactful clinical trials.



Instructors: David M. Shade, JD
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What you'll learn
Design and implement clinical trials
Collect, manage, and analyze data
Conduct trial monitoring and quality assurance
Recruit and retain clinical trial particpants
Overview
Skills you'll gain
- Clinical Data Management
- Data Collection
- Data Governance
- Statistical Reporting
- Data Cleansing
- Quality Assurance
- Scientific Methods
- Regulatory Compliance
- Clinical Research
- Biostatistics
- Data Quality
- Data Compilation
- Statistical Analysis
- Healthcare Ethics
- Clinical Trials
- Data Sharing
- Sample Size Determination
- Data Management
- Data Integrity
Tools you'll learn
What’s included

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Advance your subject-matter expertise
- Learn in-demand skills from university and industry experts
- Master a subject or tool with hands-on projects
- Develop a deep understanding of key concepts
- Earn a career certificate from Johns Hopkins University

Specialization - 4 course series
What you'll learn
Evaluate and select clinical trial designs
Implement bias control measures
Randomize participants into groups
Define clinical trial outcomes
Skills you'll gain
What you'll learn
Collect and manage clinical trials data
Assemble and share clinical trials data
Conduct statistical performance monitoring
Perform quality assurance for clinical trials
Skills you'll gain
What you'll learn
Detect and respond to protocol events
Recognize and respond to misconduct
Safeguard participant safety and trial integrity
Develop and maintain study documents
Skills you'll gain
What you'll learn
Calculate clinical trial sample size
Monitor clinical trial performance
Analyze results from clinical trials
Communicate results from clinical trials
Skills you'll gain
Earn a career certificate
Add this credential to your LinkedIn profile, resume, or CV. Share it on social media and in your performance review.
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Frequently asked questions
It typically takes about four months to complete this specialization, but learners are free to work at their own pace.
We recommend that learners have some familiarity with basic scientific, statistical, and management concepts.
The sequence provided is optimal, but not required.
More questions
Financial aid available,