Organization of Investigator’s Training Meetings
Equipping investigators and site teams with the knowledge and clarity required for consistent, compliant study execution.
Scope of Investigator Training Meetings : Establishing a strong operational foundation and reducing start-up risk.
We design and conduct structured Investigator Training Meetings (ITMs) to ensure investigators and site teams are fully prepared prior to study initiation. These meetings establish a strong operational foundation, reinforce protocol adherence, and promote standardized study conduct across all participating sites, reducing start-up risk and variability.
Training Planning and Execution
- Planning and conduct of comprehensive investigator training sessions prior to study initiation
- Coordination of training logistics and participation for investigators and site staff
Protocol and Study Overview
- Detailed review of study objectives, endpoints, eligibility criteria, and study workflows
- Clear explanation of investigator roles, site responsibilities, and study expectations
Operational and Data Management Training
- Hands-on training on CRF completion, data entry processes, and query management
- Guidance on documentation standards to ensure accurate, complete, and consistent data capture
Regulatory and Ethical Compliance
- Training on GCP principles, regulatory requirements, and patient confidentiality
- Reinforcement of ethical conduct and compliance expectations
Interactive Engagement and Alignment
- Facilitated discussions to address site-specific queries and operational challenges
- Ensuring uniform understanding and alignment across all participating sites prior to study start
