Remote Clinical Trials Internship at Siemens Healthineers
Ready to step into the world of clinical research from anywhere? This Clinical Trials Internship offers an exciting Remote Internship experience with global exposure at Siemens Healthineers. Designed for ambitious students, this internship in the USA allows you to gain hands-on clinical research experience, build regulatory knowledge, and accelerate your career in life sciences. If you’re seeking a high-impact internship opportunity for life science graduates, this role is your gateway into the clinical trials industry.
About Siemens Healthineers
Siemens Healthineers is a global leader in medical technology with over 72,000 employees across 70+ countries. The company is dedicated to advancing healthcare through innovative solutions that improve patient outcomes. A Siemens Healthineers Career offers opportunities to work on impactful projects, making it an excellent choice for a Clinical Trials Internship and an internship opportunity for life science graduates.
Internship Details
- Internship Title: Clinical Trials Internship
- Location: Malvern, Pennsylvania, United States of America
- Category: Internal Services
- Job ID: R-27704
- Job Type: Full-time, Intern (Fixed Term)
Clinical Trials Internship Overview
The organization is committed to pioneering breakthroughs in healthcare for everyone, everywhere, sustainably. It fosters an inspiring and caring environment that forms a global community celebrating diversity and individuality. Employees are encouraged to step beyond their comfort zones, with access to resources and flexibility that support both professional and personal growth while valuing unique contributions.
Role Summary
The position is designed for individuals acquiring further qualifications toward a Bachelor’s degree while gaining practical experience across technical fields through structured assignments.
Siemens Healthineers is seeking a Summer Intern to support its Clinical Trials team. The intern will gain hands-on experience in clinical trial activities, ensuring regulatory requirements are met and compliance with standard operating procedures is maintained. The role offers a flexible and dynamic work environment that encourages development beyond conventional boundaries.
Note: This is a fully remote internship opportunity.
Key Responsibilities
- Assist 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.
- 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.
- Monitor and ensure team compliance with all standard operating procedures.
Required Skills and Education
- Currently pursuing a BS or MS in Life Sciences.
- Comfortable working fully remotely during the summer.
- Strong desire and motivation to build a career in the clinical trials field.
- Demonstrates strong attention to detail and organizational skills.
- Proficient in Microsoft Excel.
- Minimum 3.0 GPA (preferred).
Compensation and Benefits
The hourly pay range for this position is $24–$40, with actual compensation varying based on education, skills, and experience. Interns are eligible for paid time off. This is a functional posting, and applicants will be considered for all internship opportunities within this functional area across the organization. Qualified candidates will be contacted directly regarding specific roles or projects.
Application Process and Timing
Applications are accepted on a rolling basis, beginning in early Fall through approximately March, depending on business needs. Candidates may not receive immediate responses and will remain under consideration for relevant opportunities unless they withdraw their application or are otherwise notified.
