When answering this question, focus on your direct involvement in clinical trials, highlighting specific phases (Phase I-IV) you have worked on. Discuss your responsibilities, such as designing the trial, monitoring patient safety, data collection, and analysis. Provide examples of successful trials you have contributed to and any challenges you overcame. Emphasize your understanding of regulatory requirements and Good Clinical Practice (GCP) guidelines. For example:
"In my previous role at XYZ Pharma, I was involved in Phase II and III clinical trials for a new oncology drug. I was responsible for designing the trial protocol, coordinating with clinical sites, and ensuring compliance with GCP guidelines. One of the key challenges was patient recruitment, which we overcame by collaborating with patient advocacy groups. The trial was successful, leading to the drug's approval by the FDA."
Stand out from the crowd with video applications! Make your video applications in minutes and show the real you.