• 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.

• 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.

• Real-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.