Regulatory Co-Op

Company:  Beam Therapeutics Inc.
Location: Cambridge
Closing Date: 02/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Company Overview
Beam Therapeutics is committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform that includes a suite of gene editing and delivery technologies and is in the process of building internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of potential therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
Beam is looking for a highly energetic and curious Co-op to join our growing regulatory team from January through June 2025. The co-op will be responsible for supporting regulatory strategy while learning about the role of regulatory affairs in biotherapeutics development. The co-op will be involved in setting and executing a regulatory strategy for novel gene editing programs. This may include activities like regulatory precedent research, regulatory interaction planning, and submissions preparation. The co-op will also have a chance to learn about and support other areas of regulatory affairs including CMC, labeling, and operations.
Responsibilities:
  • Assist the regulatory strategy leads in setting, supporting, and executing regulatory activities.
  • Support improvement and implementation of regulatory processes including chronology logs, trackers, and research regulatory precedent and competitive intelligence.
  • Participate in cross-functional meetings and discussions as appropriate.
  • Learn about and support other regulatory functions including CMC, Operations, and Labeling.
Qualifications:
  • Pursuing a bachelor's degree in a medical or scientific field.
  • Demonstrated ability to analyze and present strategy, either through coursework or leadership position in a student or civic organization.
  • A team player who is curious, motivated to learn, organized, and has excellent communication skills.
  • Note, this role will function within a hybrid (partially remote, partially onsite) working environment, and requires a self-motivated individual.
Apply Now
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