
Training and Information Coordinator Analytical Research Coordinator with 6+ years of experience in clinical and academic research and 3 years in post-grant application process and budgets. Capacity to implement a project plan and provide overall project coordination, including progress tracking and reporting, quality control, research curriculum development and training. Knowledgeable of research protocols, IRB/IACUC, ethical principles on the protection of human subjects, and protocol deviations on a variety of databases and systems. Performance history of preparing audits and internal review, conducting follow-through to resolve actionable issues, and working with principal investigators to provide guidance and training on their research and grant applications. Knowledge of grant and research agencies. Equipped with absolute integrity and professionalism.
Good Clinical Practices
Research SOPs understanding
Informed consent
Study protocols
Trial management
Project Management
Data Collection
Collaboration
Time Management
Proposal management
Training and Development
Written Communication
Good Telephone Etiquette
Decision Making
Budget