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