Responsibilities Support CRAs with the setup, monitoring, and closeout of clinical trials in accordance with Good Clinical Practice (GCP), ICH guidelines, and company SOPs. Assist in site qualification, initiation, and monitoring visits. Review and track clinical trial documentation, ensuring accuracy and completeness.Collaborate with cross-functional teams to address study-related issues.Participate in team meetings and contribute to process improvement initiatives.Qualifications Currently enrolled in a relevant degree program such as [list relevant majors - e.g., Life Sciences, Biology, Nursing, Public Health] Strong interest in clinical research and drug development. Excellent organizational and time management skills.Detail-oriented with high standards for accuracy. Ability to work independently as well as within a team environment.Proficient in Microsoft Office Suite.What You'll GainReal-world exposure to the clinical research process. Mentoring and guidance from experienced CRAs.Opportunity to network with industry professionals. Potential academic credit (if applicable with your program). Potential for future employment opportunities within our company.Please use the below link for job application and quicker response.https://lifelancer.com/jobs/view/a95911344bc31c7074733ed0fb553704