Regulatory Affairs Coordinator
13 hours ago
{"Position Overview": "Beam Therapeutics is seeking a highly motivated and detail-oriented 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.", "Responsibilities": "
\tAssist the regulatory strategy leads in setting, supporting, and executing regulatory activities.
\tSupport improvement and implementation of regulatory processes including chronology logs, trackers, and research regulatory precedent and competitive intelligence.
\tParticipate in cross-functional meetings and discussions as appropriate.
\tLearn about and support other regulatory functions including CMC, Operations, and Labeling.
", "Qualifications": "
Pursuing a bachelor's degree in a medical or scientific field.
\tDemonstrated ability to analyze and present strategy, either through coursework or leadership position in a student or civic organization.
\tA team player who is curious, motivated to learn, organized, and has excellent communication skills.
", "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.", "Key Responsibilities": "
\tSupport the development of regulatory strategies for novel gene editing programs.
\tConduct research on regulatory precedent and competitive intelligence.
\tAssist in the preparation of regulatory submissions.
\tLearn about and support other areas of regulatory affairs including CMC, labeling, and operations.
"}
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