Intern, Clinical Safety
Position Overview
This internship offers a hands-on opportunity to gain practical experience in the processes that ensure the safety of our medical devices and therapeutic products throughout clinical development. The intern will develop a comprehensive understanding of safety review workflows and contribute to various activities aimed at identifying, reviewing and adjudication of adverse event data.Job Duties1. Gain working knowledge of safety review workflows including adverse event and technical event review, CEC adjudication and MedDRA coding of adverse events.2. Assist in the execution and documentation of clinical safety reviews for ongoing studies.3. Contribute to continuous improvement initiatives for safety review processes and documentation practices.4. Support the preparation and review of safety documentation (e.g., narratives, source documents for CEC meeting, and review meeting minutes)
- 1. Currently pursuing a degree in Medicine, Life Sciences, Public Health, Nursing, Pharmacy, or related field (graduate students preferred)2. Strong interest in clinical safety, or clinical research3. Excellent attention to detail and organizational skills4. Strong written and verbal communication skills5. Ability to work independently and collaboratively in a fast-paced environment6. Proficiency in Microsoft Office (especially Excel and Word)What you will gain1. In-depth exposure to safety workflows across the clinical trial lifecycle.2. Experience working in a highly collaborative environment within a regulated industry.3. Insight into how clinical safety decisions impact patient protection.4. Opportunities to build professional skills and network with cross-functional teams.Physical1. Extended periods of computer use2. Extended periods of sitting, standing, or speaking3. Light lifting, up to 25 lbs.#LI-DNI