Clinical Research Associate

• 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.

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