Pharmaceutical Senior Legal Research Associate
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Before you apply
Salary$75k – $80k
LocationRemote (United States)
Work moderemote
Typefull-time
SenioritySenior
Experience3+ yrs
DepartmentSoftware
Company size8+ people
First seenOct 16, 2026 · 2w ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
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
Familiarity and comfortability in working with technology and software is a must
Professional certifications in pharmaceutical compliance (e.g., RAC) are a plus
Skills
Microsoft Word
Google Drive
Benefits
PTO
Paid holidays
Health insurance
Dental insurance
Vision insurance
Life insurance
Short term disability
Long term disability
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 the company
About LighthouseAI
LighthouseAI, a Pharma Solutions company, provides state licensing software and professional services to pharmaceutical and medical device manufacturers, wholesale distributors, third-party logistics providers (3PLs), and pharmacies. Our software identifies the licensing requirements that apply to each facility, monitors regulatory change, and tracks every license and renewal across 56 US jurisdictions. Our 35+ veteran licensing professionals handle filings, renewals, and agency communication. Since 2015, we have served 700+ clients and today manage 13,000+ licenses for 250+ active clients.