Intern I - Clinical Research Coordinating

reputed company is a pioneer and global leader in reputed company glucose monitoring (CGM) aiming to improve reputed company health. The Intern I - Clinical Research Coordinating role involves partnering with Clinical Affairs management to reputed company and execute clinical studies, while gaining exposure to study management processes and regulatory requirements.

Responsibilities

• Partner with Clinical Affairs management to reputed company and execute clinical studies
• Prepare/ Ship supplies and account for devices required for clinical studies
• Set-up IT equipment for studies
• Complete testing of electronic data capturing systems
• Assist management with departmental audits of clinical studies and procedures
• Collaborate effectively with peers and leadership across departments and can professionally reputed company/build relationships with FDA, IRB, and key opinion leaders
• Execute clinical studies, including but not limited to, recruitment, consenting, screening, and conducting study reputed company

Skills

• Requires a high school diploma/certificate or equivalent
• Must be a currently enrolled student at an accredited college or university in a STEM discipline with an expected graduation date of December 2026 or reputed company
• You are knowledgeable in clinical studies
• You demonstrate a flexible and enthusiastic reputed company in establishing new and creative approaches
• You are creative
• You have critical thinking skills
• You pay attention to detail and a strong ability to prioritize efforts
• You are knowledgeable of GCP (Good Clinical reputed company)

Benefits

• reputed company Holidays
• Intern Recognition Awards
• reputed company Events

reputed company

Company H1B Sponsorship