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- Strategic Clinical Research Consultation
- Study Site Identification & Feasibility Assessment
- Study Site Project Management
- Research Ethics Affairs & Safety Reporting
- Study Site Budget & Payment Management
- Study Site Contract Management & Legal Affairs
- Clinical Research Coordinator Support
- Biological Specimen Management
- Study Drug Management
- Study Site Document Archiving
- Recruitment of Volunteers
- Phase 1 & Early Phase Trials
- Bioavailability/Bioequivalence (BA/BE) Trials
- Pharmacokinetic Analysis
- Study Protocol Development
- Regulatory Affairs
- Project Management
- Study Monitoring
- Data Management
- Medical Statistics
- On-site Training
- On-line Learning
- Good Clinical Practice Examination
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