As an intern in the RMW department, you have the opportunity to learn how to write high quality clinical documents to support the development, regulatory approval, and maintenance of our products. These documents include investigator’s brochures, clinical trial protocols, and clinical study reports, as well as summaries of efficacy and safety and responses to health authority questions. How you can make a difference: Apply your excellent writing skills, ability to interpret and summarize statistical and medical information and attention to detail to the design of our clinical trials and reporting of our data.

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Qualifications:

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• Candidates must be legally authorized to work in the U.S. and must not require sponsorship for employment visa status now, or in the future (e.g., H1‑B).
• Candidate must be actively enrolled in an accredited University for the duration of an intern assignment pursuing a Bachelor’s, Master’s, Pharm D, and/or Ph.D.
• Completion of Undergraduate sophomore year at accredited University is required.
• Availability to work 40 hours per week.
• A GPA of 3.5 or better.

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Education Preferences:

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Preferred fields of study are biological science or another health-related scientific or medical field.

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