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This is a full-time remote position. Working hours: Monday-Friday 8am - 4:30pm ET Essential Duties and Responsibilities: • Research:  Research and review and interpretation of statutes, laws, legislation, rules, emergency orders, etc.). Familiarity with various state agencies across the life sciences industry. • Collaboration:  Offering insight and ideas for improvements within the team and the software so that we as a team are always improving. • Communication:  Lead team communication with the various boards of pharmacy and other regulatory agencies governing the pharmaceutical supply chain. • Organization:  Stay organized while effectively prioritizing multiple projects at once. • Time Management:  Strong time management skills to complete projects by deadlines. • Efficiency:  Self-motivated individual who takes ownership of their projects. • Technology Skills:  Familiarity and comfortability in working with technology and software is a must. • Responsibilities and tasks outlined in this document are not exhaustive and may change as determined by the needs of the company and/or it’s clients. Work Experience Qualifications: • 3+ years of experience researching federal and state law as well as regulatory resources within the drug supply chain or pharmacy regulatory affairs. • Experience with conducting a state-by-state assessment of licensing requirements based on business model and product portfolio. Other Qualifications: • Strong knowledge of pharmaceutical regulations, such as FDA regulations and state board of pharmacy regulation. • Excellent research and analytical skills, with the ability to learn and interpret complex regulatory requirements and communicate them effectively. • Proven ability to work collaboratively with cross-functional teams and provide expert guidance on compliance matters. • Strong attention to detail and a commitment to accuracy in all compliance-related activities. • Ability to adapt to changing regulatory landscapes and stay updated with industry developments. • Professional certifications in pharmaceutical compliance (e.g., RAC) are a plus. • Ability to self-manage and prioritize efforts effectively across multiple projects at once. • High attention to detail. • Strong time management skills to complete projects by deadlines. • Self-motivated individual who takes ownership of their projects. • Administrative skills (basic Microsoft Word skills and Google Drive required). • Logical and critical thinking a must. • Maintain excellent verbal, writing, and language skills. Supervisory Responsibilities: This position has no direct supervisory responsibilities but is designed with an expectation of a leader that embodies and represents the Company's culture. Further, there are continuing opportunities for advancement within our growing Company and affiliated companies. Salary Range:  $75,000 - $80,000 Benefits offered include: • PTO & Paid Holidays • Health, Dental, Vision Insurance • Life Insurance • STD / LTD About LighthouseAI LighthouseAI provides pharmaceutical state licensing software and services to pharmaceutical manufacturers, wholesale distributors, logistics companies, and pharmacies. The LighthouseAI product suite includes LighthouseAI Intelligence®, which uses artificial intelligence to automate compliance requirement research, and LighthouseAI Management® which enables maintenance. LighthouseAI creates a stress-free and streamlined state licensing experience with support from our expert industry veterans and professional solutions.