Clinical Research Associates (CRAs) play a vital role in overseeing clinical trials. They monitor the progress of trials, ensuring compliance with regulations and good clinical practice (GCP) guidelines. CRAs work closely with research sites, verifying data accuracy and patient safety. This career is ideal for those with a strong understanding of clinical trials and a meticulous approach.

• Key Responsibilities: Site management, data verification, regulatory compliance.
• Skills Required: Clinical trial knowledge, monitoring skills, attention to detail.