Pharmaceutical Senior Legal Research Associate

LighthouseAI

11d•$75,000 - $80,000•Remote

About The Position

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.

Requirements

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.
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.
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.

Nice To Haves

Professional certifications in pharmaceutical compliance (e.g., RAC) are a plus.

Responsibilities

Research and review and interpretation of statutes, laws, legislation, rules, emergency orders, etc.
Offering insight and ideas for improvements within the team and the software
Lead team communication with the various boards of pharmacy and other regulatory agencies governing the pharmaceutical supply chain.
Stay organized while effectively prioritizing multiple projects at once.
Complete projects by deadlines.
Self-motivated individual who takes ownership of their projects.
Familiarity and comfortability in working with technology and software