2027 Co-Op, Safety Epidemiology
About The Position
Moderna is seeking a highly motivated PhD or ScD student to join its Global Safety Epidemiology program for a Spring/Summer co-op running from January 18, 2027 through June 25, 2027. Applicants must be available for the full program. The role offers hands-on experience in real-world epidemiologic research, safety monitoring, signal evaluation, and integrated evidence planning in a regulated biopharmaceutical environment. The co-op will gain exposure to epidemiology in pharmacovigilance across the development lifecycle, contribute to safety research and evidence generation, and work with cross-functional teams. The role follows Moderna’s 70/30 work model, with 70% of work in-office. Candidates must already have U.S. work authorization that they can maintain without future sponsorship. Due to export-control requirements, only individuals who qualify as U.S. persons are eligible.
Requirements
- Currently enrolled in a PhD or ScD program in Epidemiology or a closely related discipline.
- Strong background in epidemiology and biostatistics.
- Experience with SAS or R.
- Must be available for the full co-op program, January 18, 2027 through June 25, 2027.
- Must already hold U.S. work authorization and be able to maintain it without future sponsorship.
- Must qualify as a U.S. person under applicable export-control requirements.
Nice To Haves
- Interest in vaccine development, pharmacoepidemiologic methods, pharmacovigilance, and data-driven decision-making.
- Ability to meet deadlines, a 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.
- Desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
Responsibilities
- Conduct epidemiologic research to contextualize and evaluate safety signals, important potential risks, and populations relevant to safety monitoring, such as pregnant women.
- Contribute to evidence generation and synthesis for vaccine safety monitoring in key global markets outside the United States.
- 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, such as characterizing the incidence of one or more safety topics of interest.
Benefits
- Free premium access to meditation and mindfulness classes.
- Subsidized commuter benefits.
- Paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown.
- Location-specific perks and extras.
- May be eligible for an annual discretionary bonus, other incentive compensation, or an equity award, subject to plan eligibility criteria and individual performance.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
Ph.D. or professional degree
