Certified Professional in Clinical Research Coordination
-- viewing nowCertified Professional in Clinical Research Coordination (CPCRC) certification validates your expertise in clinical trials. This program is for clinical research coordinators, clinical research assistants, and study managers.
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Course details
• Clinical Trial Design and Methodology
• Regulatory Affairs and Compliance
• Case Report Form (CRF) Design and Data Management
• Patient Recruitment and Screening
• Adverse Event (AE) and Serious Adverse Event (SAE) Reporting
• Medical Terminology and Pharmacology
• Data Integrity and Quality Control
• Clinical Trial Monitoring and Auditing
• Communication and Interpersonal Skills
Career path
Certified Professional in Clinical Research Coordination (CRC) Job Market Trends UK
Career Role | Description |
---|---|
Clinical Research Associate (CRA) | On-site monitoring of clinical trials, ensuring data integrity and regulatory compliance. High demand for CRAs with strong GCP knowledge. |
Clinical Research Coordinator (CRC) | Management of daily trial activities, including recruitment, data collection, and patient follow-up. Essential role in successful trial execution. |
Clinical Trial Manager (CTM) | Oversees all aspects of a clinical trial, from planning and budgeting to execution and reporting. Requires extensive experience and leadership skills. |
Entry requirements
- Basic understanding of the subject matter
- Proficiency in English language
- Computer and internet access
- Basic computer skills
- Dedication to complete the course
No prior formal qualifications required. Course designed for accessibility.
Course status
This course provides practical knowledge and skills for professional development. It is:
- Not accredited by a recognized body
- Not regulated by an authorized institution
- Complementary to formal qualifications
You'll receive a certificate of completion upon successfully finishing the course.
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