About The Position

This is a full-time summer internship based in Cambridge, MA from June 7, 2027 – August 20, 2027. Candidates must be available for the entire duration of the program. We are seeking a highly motivated PhD/ScD student to join our Global Safety Epidemiology program, providing a unique opportunity to gain hands-on experience in real-world epidemiologic research, safety monitoring, signal evaluation, and integrated evidence planning in a regulated biopharmaceutical environment.

Requirements

  • Currently enrolled in a PhD or ScD program in Epidemiology or a closely related discipline.
  • Strong background in epidemiology, biostatistics
  • Experience with SAS or R
  • Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

Nice To Haves

  • Interest in vaccine development, pharmacoepidemiologic methods, pharmacovigilance, and data-driven decision-making.
  • Ability to meet deadlines, team-oriented mindset, adaptability under pressure, and a proactive approach to problem-solving.
  • Demonstrated ability to work independently while contributing effectively within a team environment.
  • Strong written and verbal communication skills.
  • High attention to detail and commitment to quality and compliance.
  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Responsibilities

  • Gain exposure to the role of Epidemiology in pharmacovigilance across the development lifecycle.
  • Conduct epidemiologic research to contextualize and evaluate safety signals, important potential risks, and special populations relevant to safety monitoring (e.g., pregnant women).
  • Contribute to evidence generation and synthesis for vaccine safety monitoring in key global markets outside the US.
  • Engage with cross-functional teams, including Clinical Safety and Pharmacovigilance, Real-World Evidence Analytics, Medical Affairs, Health Economics & Outcomes Research, and Clinical Development.
  • Contribute to cross functional signal detection, validation, and evaluation workflows.
  • Lead and present findings from an epidemiologic project addressing a topic relevant to safety monitoring (e.g., characterizing incidence of one or more safety topics of interest).

Benefits

  • Free premium access to meditation and mindfulness classes
  • Subsidized commuter benefits
  • Generous paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown
  • Location-specific perks and extras

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What This Job Offers

Job Type

Full-time

Career Level

Intern

Education Level

Ph.D. or professional degree

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