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Intern – Global Regulatory Sciences
Oncology, Cardiovascular, CV, And Neuroscience, Ns, Summer 2023
Confirmed live in the last 24 hours
Locations
Princeton, NJ, USA
Experience Level
Intern
Desired Skills
PowerPoint/Keynote/Slides
Communications
Requirements
  • College senior or Graduate student in a Life Sciences Program such as Molecular Biology, Biochemistry, Chemistry, Chemical Engineering, Biomedical Engineering, Pharmacy. Understanding of the pharmaceutical industry is preferred
  • Demonstrates a high-level of self-motivation and professional commitment
  • Attention to detail, excellent organization skills, good verbal and written communication skills are required
  • Ability to rapidly adapt to different issues and projects at one time. Good interpersonal skills
  • Ability to work independently on routine assignments with daily check-ins and to work cooperatively with senior staff providing key assistance on complex assignment
  • Willingness and ability to effectively work in a matrixed team environment
  • Computer experience must include familiarity with Word, Excel and PowerPoint
Responsibilities
  • Work with Engagement Manager and team to learn and contribute to Regulatory documents/deliverables/submissions including, but not limited to:
  • HA interactions (meeting requests/meeting packages, meeting preparation, rehearsals, execution, follow-up, minutes, etc.)
  • IND, BLA, and NDA original/supplemental/maintenance submissions
  • Safety and Annual report submissions
  • Rapid response team meetings to ensure quality and timely responses to health authority queries according to the rapid response process. This includes the preparation of the strategy for the response to HA queries
  • Global submission plans and supporting those plans can be executed on time
  • Attend and participate in various Regulatory Strategy, Therapeutic Area-related, and matrix team meetings as needed
  • Manage and prioritize multiple complex projects to support organization and enterprise initiatives
  • Drive operational excellence in Global Regulatory Strategy & Policy through projects aimed to support collaboration and improve efficiency
  • Develop a comprehensive understanding of the pharmaceutical industry, and different functions within drug development
Bristol-Myers Squibb

10,001+ employees

Biopharmaceutical development company
Company Overview
Bristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.