Intern, Legal

EndoHazelwood, MO
5dHybrid

About The Position

The Program Par Health offers an 11-week internship program designed to provide an immersive experience in the pharmaceutical industry. As a Par Health Intern, you’ll have the chance to contribute to meaningful projects that align with your field of study. This program allows you to apply classroom knowledge in a real-world corporate setting while building valuable connections through networking opportunities across the organization. Summary of Position The Legal Intern will support Par Health’s Legal Department across a variety of matters affecting a global pharmaceutical organization. This role provides exposure to regulatory, compliance, and commercial legal issues, allowing a law student to gain hands on experience in a highly regulated environment. The Legal Intern will assist attorneys with research, drafting, and project-based work that contributes directly to the company’s mission of delivering quality and essential medicines.

Requirements

  • Must be currently enrolled in an accredited JD program with completion of at least one year of law school prior to the start of the internship.
  • Demonstrated interest in healthcare or pharma.
  • Strong legal research and writing skills, including ability to analyze laws and summarize findings.
  • Excellent organizational skills with the ability to manage multiple tasks and deadlines.
  • High attention to detail and accuracy, particularly in reviewing legal documents.
  • Willingness to work in a hybrid environment, including reporting to the office at least two days per week to support collaboration, training, and engagement with management and internal stakeholders.
  • Experience with MS Office (Word, Outlook, PowerPoint, Excel, Teams, etc.) and comfortable with learning new technology platforms.
  • Motivated self-starter, operates independently, and possesses the ability to handle confidential information with discretion and sound judgment.
  • Strong interpersonal and communication skills with the ability to interact with internal and external partners professionally.

Responsibilities

  • Conduct legal research on issues related to FDA regulations, state licensing, pharmaceutical marketing, manufacturing, privacy, and other healthcare compliance topics.
  • Assist with drafting and reviewing contracts, policies, and other legal correspondence.
  • Support the ongoing rollout of the Contract Pod AI (CPAI) platform, including learning system functionality and assisting with cross-functional integration efforts and user training.
  • Help track and organize legal matters, including contract workflows and regulatory filings.
  • Collaborate with cross-functional teams such as Regulatory Affairs, Quality, Government Affairs, and Commercial.
  • Participate in meetings, prepare summaries, and contribute to special projects as assigned.
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