Clinical Trials Internship
About The Position
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Acquires further qualification for a Bachelor's degree, and gathers respective working experience in different technical fields of expertise, in the course of a respective assignment. Siemens Healthineers is seeking a Summer Intern to assist our Clinical Trials team. As a clinical trials intern, you will gain hands-on experience supporting clinical trial activities ensuring regulatory requirements are met and compliance with standard operating procedures. We provide a flexible and dynamic work environment that encourages personal and professional development beyond conventional boundaries. If you are interested in contributing to our global team as a Clinical Trials Intern, we invite you to apply. PLEASE NOTE: This is a fully remote internship opportunity This is a role well suited for a highly motivated student looking to build their skill set and gain hands-on experience.
Requirements
- Pursuing a BS or MS in Life Sciences or Health Science degrees
- Comfortable working completely remote for the summer
- Strong desire and motivation to develop a career in the clinical trials space
- Possess strong attention to detail, and organization skills
- Proficient in Microsoft Excel
- Minimum 3.0 GPA (preferred)
- This position is open to candidates who are permanently authorized to work in the United States.
- We are unable to support visa sponsorship for this role now or in the future, including for those currently utilizing F-1/OPT, H-1B, or other employment-based work visas.
Responsibilities
- Assisting with monitoring visit preparation using CTMS, ensuring all required documentation is ready for site monitoring visits.
- Provide administrative and organizational support for Clinical Study Report (CSR) development for a new study.
- Help configure templates for invoicing, visit letters, and other essential documents in CTMS and eTMF systems.
- Maintain and update training records for study team members, ensuring compliance with SOPs and regulatory requirements.
- Contribute to the development of clinical study reports as needed
- Monitoring and ensuring the team is in compliance with all standard operating procedures.
Benefits
- Siemens Healthineers offers interns paid time off.
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What This Job Offers
Career Level
Intern
Number of Employees
5,001-10,000 employees
