Global Reg Affairs Intern

What you'd do

• Work on programs and strategies for compounds in development and/or marketed products.
• Gain experience and exposure in drug development intended to address unmet medical needs in markets globally through an understanding of laws, guidance documents, and regulatory requirements for drugs and combination products.
• Use creative problem solving skills to develop new ideas and insights, including takeaways about yourself as a leader.
• Partner with other regulatory interns with diverse skills and experiences in building solutions for real-life business challenges through hands-on projects.

What they want

• Earned or is currently pursuing an advanced degree in scientific, technology or engineering related field from an accredited academic institution.
• Examples include, biomedical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy or other healthcare science.
• Strong academic track record is required.
• Experience/interest in graphic or visual design, journalism, creative writing, or creative arts is a plus.
• Demonstrated leadership in campus/community activities is desired.
• Able to work independently and collaboratively as part of a group, demonstrating curiosity and flexibility.
• Possess a “can do” approach, and courage to speak your voice and suggest innovative ideas.
• Available to work full-time (40 hours per week) during internship.
• Candidate must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.g. H1-B status) now or in the future.
• Desired assignment location is Pennsylvania or New Jersey and may require local travel. Flexible arrangements in other U.S. locations may be considered.