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Clinical Research
Services and Consulting
Clinical Project Management
Feasibility / Capability Research
Clinical Trial Contract Management
Ethics Committee / Regulatory Approval Management
Patient Recruitment Management
Clinical Research Monitoring
Risk Based / Centralized Statistical (Remote) Monitoring
Regulatory Affairs
Quality Assurance
Auditing
Training & Education
Data Management
Pharmacovigilance
Investigational Product Logistics & Destruction
Biological and Clinical Data Analysis / Statistics
Medical Writing, Translation Services
Clinical / Medical Professionals Resourcing (Outsourcing, Executive Search)
Medical Device Studies
Training and Education
a) For Clinical Research Associate job seekers
Fundamentals of Clinical Research Monitoring
Good Clinical Practice (GCP) principles
The role of Clinical Research Associate (CRA) in clinical research
Regulatory requirements for clinical research
Clinical research methodology and its role in pharmaceutical development
Monitoring clinical trials to ensure valid and useful study data
Investigator selection and evaluation
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b) For Hospitals (Investigators, Study Coordinators, Study Nurses)
GCP and Clinical Trial Conduct Training
Good Clinical Practice (GCP) principles
The role of a clinical research investigator in clinical research
Regulatory requirements for clinical research
Clinical research methodology and its role in pharmaceutical development
Preparation for site audit
Clinical trial documentation management
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