The Junior Clinical Research Associate training by ECCRT has equipped me with a clear understanding of the clinical research lifecycle and CRA roles, and site monitoring skills for identifying non-compliance and ensuring data integrity. These skills will improve my effectiveness as a junior clinical research associate. I will apply my site monitoring skills to identify non-compliance

I definitely achieved a better understanding of what and why I need to implement to achieve better sponsor oversight. I was lucky to attend a very small group (3 participants), therefore it was a very interactive session and all participants could present their issues and experiences with oversight which Paula could focus on.

The high quality face-to-face approach: Kevin and Lisbeth provided a safe professional environment to dive deep into questions. All trainees job specific challenges were covered by the trainers perspectives, who were eager to conduct the training in a practical way for the trainees daily experience.

I expected to understand the difference between device and drug trials and I feel that due to this course I have obtained that knowledge. I hope to now also to start managing device studies as a consultant. The group was very pleasant and interactive. The diverse backgrounds of the group helped to get different views on

I have gained new knowledge of the chemical control of production and the regulations governing the introduction of a product into Phase I First-In-Human, and I have expanded and enriched my knowledge of the regulations and principles of planning experiments at non-clinical and preclinical stages of development. I intend to complete the requirements based on the

I enjoyed the project planning activities and budgeting activities. I have been working in this field for almost 2 years and this helped structure in my mind all I have seen up to this point. I appreciated the applicable content, nicely structured and interesting discussions with other professionals during the activities.

I have done a couple of courses from ECCRT now and the course content/materials are very well prepared. Trainers are super experienced and friendly. I always feel very welcome and appreciated when I participate with questions or by sharing work experiences that bring value to the discussion.

Between the ICH GCP course and this course I learned a lot. Not only the theoretical part, but I also have a clearer idea of what a CRA is doing daily and of all the steps and documentation about clinical trials. I hope that this knowledge gives me a burst in finding a job, in which

The training equipped me with knowledge of clinical trial processes, study procedures, and regulatory requirements. It improved my skills in conducting monitoring visits, completing eCRFs, and identifying protocol deviations. It also reinforced the importance of adhering to GCP guidelines, proactive problem-solving, and effective communication. The main point I will apply in practice is improving effective communication