Regulatory Affairs Intern 2026
About The Position
Maze Therapeutics is seeking a Regulatory Affairs Intern to join the team as part of this year’s Summer Internship Program. This internship offers hands-on involvement in regulatory activities that inform program evaluation and clinical development decisions within a company advancing precision medicines informed by human genetics. The intern will report to the Senior Director, Regulatory Affairs and collaborate cross-functionally to support development workstreams. This position requires an onsite presence of 5 days per week to support team engagement and regulatory activities. As an intern at Maze, you will work closely with experienced industry professionals and gain valuable, hands-on, full-time work experience. Working closely with the Regulatory Affairs team and cross-functional partners, you will contribute to meaningful projects that integrate regulatory strategy, community engagement, and scientific communication.
Requirements
- Strong interest in Regulatory Affairs and global drug development
- Analytical ability and capacity to synthesize complex scientific or technical information
- High attention to detail and organizational skills
- Excellent written and verbal communication skills
- Ability to work onsite 3–4 days per week during the internship
Nice To Haves
- Enrollment in a degree program in life sciences, biotechnology, regulatory science, or a related field
- Coursework or research experience related to drug development, clinical research, or the biomedical sciences
- Ability to work independently while also contributing effectively as part of a team
- Intellectual curiosity and comfort engaging with complex scientific or regulatory concept
Responsibilities
- Develop impactful, engaging social media and digital content tailored to the APOL1 and CKD communities.
- Create the patient centric campaign, including messaging, visuals, and outreach strategy to effectively reach and resonate with diverse patient audiences.
- Support digital storytelling and awareness efforts highlighting patient voices and APOL1 education.
- Collaborate with cross functional partners to ensure all content aligns with compliance, brand, and patient centric standards.
- Track performance metrics and insights to refine content and outreach.
- Contribute to measuring the impact of community engagement activities.
Benefits
- Targeted regulatory and drug development trainings
- Leadership exposure and cross-functional collaboration
- Mentorship and professional development from industry experts
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
No Education Listed
