Spain Internship Program, Clinical Operations Intern
External
Edwards Lifesciences · SpainPrepare for this interview
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Requirements
- We are looking for a technically oriented student with curiosity, initiative, and creativity, eager to learn how clinical studies are conducted in the real world.
- Currently enrolled in a university degree enabling curricular or extracurricular internships.
- Technical background, preferably in Pharmacy or Biomedical Engineering.
- Strong attention to detail and ability to work accurately with different document types.
- Good organizational skills and ability to manage repetitive tasks in a structured manner.
- Strong written communication skills in English.
- Basic understanding of ERP systems and Good Documentation Practices.
- Interest in clinical trials, Artificial Intelligence, systems integrity, regulatory, and process improvement.
- Structured, methodical, and reliable working style.
- Ability to collaborate with cross‑functional and international teams.
Benefits
Additional Information
Spain Internship Program, Clinical Operations Intern (6 months) Make a meaningful difference to patients around the world. Our Spain Internship Program is designed to help early-career professionals contribute to solutions that transform patient lives. We also believe in investing in the future of our talented people across the globe, including early career professionals seeking to explore and establish themselves within the medical device industry. We'll provide you with the opportunity to thrive in a dynamic environment where you can make innovative contributions. As a Clinical Operations Intern with us, you'll find motivation and inspiration in a culture that emphasizes passion for patients as you discover your own strengths. Location: Valencia, Spain Duration: 6 months internship, 30-40 hours/week Recruitment process: May-August Start Date: October 1 st , 2026 Please apply in English! What to expect from your internship: Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Operation s team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will explore the evidence needed to optimize patient outcomes. How you'll make an impact: Assist in the review of clinical study documentation (e.g., EFS, pivotal studies) to support accuracy, completeness, and adherence to Good Documentation Practices (GDP), under guidance from the team. Support quality control activities by performing basic document checks and identifying inconsistencies or missing information, escalating as needed. Help organize, upload, and maintain clinical trial documents within eTMF and/or CTMS systems, ensuring alignment with internal procedures and regulatory requirements. Contribute to maintaining inspection-ready files by ensuring documents are appropriately filed, version-controlled, and traceable. Collaborate with cross-functional teams (e.g., Clinical Operations, Study Teams, Compliance) to gain exposure to end-to-end clinical trial processes.
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