Once selected, you will sign an MOU outlining your responsibilities and receive your assigned research question, marking the official start of your studentship.

Kick off the program with certified Good Clinical Practice (GCP) training to ensure you understand the ethical and procedural aspects of clinical research. 

Note: Completion of this training is mandatory to proceed.

With guidance from CRENC mentors, you will develop a comprehensive research proposal. This document will serve as the foundation for your project and ensure clarity in your objectives and methodology.

Begin implementing your approved research protocol. This phase includes hands-on training in basic statistical analysis to prepare you for interpreting your findings effectively.

Work with your mentors to analyze the data you’ve collected, using statistical tools like R, STATA, or SPSS. Gain valuable insights and prepare your findings for further application.

Document your research in the form of a master’s thesis or equivalent. This step focuses on scientific writing, ensuring your work meets academic and professional standards.

Present and defend your findings before an evaluation panel. This critical step demonstrates your understanding of the research process and your project’s impact.

Finalize and submit at least one publication based on your research. This may include a journal article, abstract, or case report. Authorship will be determined collaboratively upon submission.

Note: The publication is a mandatory deliverable for all participants.