Certified Professional in Clinical Trial Monitoring
-- viewing nowCertified Professional in Clinical Trial Monitoring (CPCM) certification validates your expertise in clinical research. It's for clinical research professionals, including monitors, CRAs, and auditors.
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Course details
• ICH-GCP Guidelines
• Clinical Trial Regulations (e.g., 21 CFR Part 11)
• Monitoring Methodology & Techniques
• Data Management & Reporting
• Risk-Based Monitoring
• Case Report Form (CRF) Review & Data Verification
• Regulatory Compliance & Auditing
• Medical Terminology & Pharmacology
• Clinical Trial Design & Statistics
Career path
Career Role: Certified Professional in Clinical Trial Monitoring (UK) | Description |
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Senior Clinical Trial Monitor | Experienced professionals leading monitoring activities, ensuring data integrity and regulatory compliance in complex clinical trials. High demand for strong GCP knowledge and risk-based monitoring expertise. |
Clinical Trial Monitoring Associate | Entry-level roles providing support to senior monitors. Focus on data verification, site visits, and reporting. Excellent opportunity for career progression within the clinical research field. |
Lead Clinical Trial Monitor | Supervisory roles managing a portfolio of trials, mentoring junior staff, and ensuring adherence to protocols and timelines. Requires extensive experience in clinical research and leadership capabilities. |
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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