Pharmaceutical Senior Legal Research Associate

Location: Remote (United States)

Department: SaaS: IRD

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 Companys 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 the Company

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.