Intern Regulatory Affairs

ErascaSan Diego, CA
262d$25 - $40Remote

About The Position

Erasca's 2025 Summer Internship Program is a paid 8-10 week internship for students looking for meaningful work experience in the biotechnology industry. We have designed the program to give interns hands-on project experience and the opportunity to develop professional skills and establish career networks and mentors. Under the mentorship of the Chief Regulatory Affairs Officer and working within the Regulatory Affairs department's team environment, the intern will have the opportunity to understand and utilize the available regulatory research tools such as FDA, EMA, and ICH websites, guidance documents and regulations to collect and summarize the status of critical and evolving regulatory topics. Additionally, the position may assist in development and implementation of processes related to regulatory affairs documentation, with the potential for evaluation of AI tools and use cases in this professional setting. These topics will be discussed and confirmed in collaboration with the intern in order to ensure an aligned level of complexity and/or interest.

Requirements

  • Candidates should be currently participating in a Regulatory Affairs-focused educational program (eg, BS or MS in Regulatory Affairs or Regulatory Science or other related area of study).
  • Prior experience in Regulatory Affairs is not required.
  • Strong skills utilizing Microsoft Office programs such as MS Word and PowerPoint.
  • Ability to read, summarize, and interpret a high volume of complex information.
  • Self-motivated, driven to learn and build a knowledgebase related to Global Regulatory Affairs.
  • Demonstrated ability to achieve goals and meet deadlines in a fast-paced environment.
  • Strong learning orientation, curiosity, and commitment to science and helping patients.

Responsibilities

  • Utilize available online resources to research critical and evolving regulatory affairs topics.
  • Provide a comprehensive summary of available information with appropriate and accurate references.
  • Working with the Regulatory Affairs department as appropriate, provide an interpretation and distillation of the collected information so that important inferences and messages are identified.
  • Assist with routine Regulatory Department projects and activities.
  • Assist in development and implementation of document archiving process/systems for regulatory department archives.
  • Assist in creation and evaluation of AI use cases for Regulatory Affairs professionals, partner with the regulatory affairs department, etc.
  • Work will be performed remotely with frequent telecommunication.
  • Perform all duties in keeping with the company's core values, policies and all applicable regulations.

Benefits

  • Paid Time Off
  • Holiday and Sick Leave
  • Medical, Dental and Vision Plans
  • Short- and Long-Term Disability
  • Basic and Voluntary Life/AD&D Coverage
  • Flexible Spending Accounts (FSA, HSA, and Commute)
  • Critical Illness and Accident Coverage
  • Pet Insurance
  • Employee Assistance Program
  • 401(k) Plan with Erasca contribution
  • Opportunity to participate in an Employee Stock Purchase Program

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What This Job Offers

Job Type

Part-time

Career Level

Intern

Industry

Professional, Scientific, and Technical Services

Education Level

Bachelor's degree

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