Intern, Regulatory Affairs (Neurology)

As an Intern in Regulatory Affairs at MCRA, you'll engage in various projects focusing on Neurology. Your responsibilities will include conducting research on specific regulatory topics, enabling you to develop a comprehensive understanding of regulatory processes in the medical device industry. You will also assist in creating a unified resource aimed at enhancing project execution and knowledge management, working closely with mentors to ensure that your contributions are impactful and educational.

To qualify for the Intern, Regulatory Affairs position at MCRA, candidates should be pursuing a degree in Biomedical Engineering or Data Science and should be either incoming Juniors or Seniors. Additionally, familiarity with OneNote, strong organizational skills, and a genuine interest in knowledge management are essential for success in this role.

The internship program for the Intern, Regulatory Affairs role at MCRA spans 8 weeks, from June 2, 2025, to July 25, 2025. During this time, you will be expected to work around 25 hours per week, allowing you the flexibility to manage your schedule while gaining valuable experience.

Interns at MCRA can expect to gain critical hands-on experience in Regulatory Affairs, particularly in the field of Neurology. Through real-world projects and mentorship from industry leaders, you'll develop a deep understanding of regulatory processes, project management, and the integration of regulatory affairs with clinical research and quality assurance.

The Intern, Regulatory Affairs position at MCRA offers a competitive hourly pay rate ranging from $20 to $20 per hour. This compensation reflects the importance of the role and the value of the experience you will gain during the internship.

In preparing your response, mention the importance of regulatory affairs in ensuring that medical devices are safe and effective. Discuss how regulatory professionals work closely with design and engineering teams to navigate compliance while managing the project effectively.

Highlight relevant coursework and projects from your Biomedical Engineering or Data Science program that relate to regulatory frameworks or analysis, showing how your education aligns with the duties of the Intern, Regulatory Affairs role.

Discuss any project management experience, including coursework or prior internships, where you managed timelines and deliverables. Highlight your organizational skills and ability to work efficiently in a team environment.

Share your experience with OneNote or similar tools, giving specific examples of how you used them for organization and information sharing during group projects or personal study.

Express your passion for neuroscience and how it connects to regulatory affairs by discussing current trends in medical devices and their impact on patient care. This shows your genuine interest in the field.

Discuss your time management strategies and how you plan to balance the internship hours with academic responsibilities, emphasizing your ability to prioritize tasks efficiently.

Prepare to describe a specific project, outlining the challenge, the actions you took to address it, and the outcome, showcasing your problem-solving skills and resilience.

Clearly articulate your goals for the internship, such as gaining hands-on experience, networking opportunities, or valuable insights into the regulatory process, showing your eagerness to contribute and learn.

Share your approach to teamwork, focusing on collaboration, communication, and how you contribute to achieving common goals.

Use this opportunity to ask insightful questions about the company culture, projects you may be involved in, or how success is measured in the intern role. This shows your proactive interest and engagement.