Intern - Project Management (clinical Supply/clinical Quality)

✨ About The Role

- The Project Management intern will provide support to the Clinical Supply Manager or the Clinical Quality Team, gaining valuable exposure to quality processes and regulatory requirements. - Responsibilities include managing clinical supply inventory, tracking quantities and expiration dates, and ensuring compliance with Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP). - The intern will assist in ensuring that clinical supplies are handled according to standard operating procedures (SOP) and other regulatory requirements. - The role offers the opportunity to learn about the drug development process and the significance of clinical trial data in advancing therapeutic products. - The internship program runs from May through August 2025, requiring the intern to be onsite in Silver Spring, MD for the entire duration.

⚡ Requirements

- The ideal candidate for this internship should be currently enrolled in a college or university program, preferably in a field related to project management, clinical supply, or quality assurance. - A strong interest in the pharmaceutical or biotech industry, particularly in clinical trials and drug development processes, is essential for success in this role. - The candidate should possess excellent organizational skills and attention to detail, as they will be responsible for managing clinical supply inventory and ensuring compliance with regulatory requirements. - Effective communication skills are important, as the intern will be collaborating with various teams and may participate in presentations or speaker series. - A proactive attitude and the ability to work independently while also being a team player will contribute to a positive internship experience.