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Pharmaceutical Senior Legal Research Associate

LighthouseAI

Philadelphia (Philadelphia County)

Remote

USD 75,000 - 80,000

Full time

Yesterday
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Job summary

A leading pharmaceutical solutions company seeks a Pharmaceutical Senior Legal Research Associate for a remote role. Responsibilities include researching regulatory requirements, collaborating with teams, and ensuring compliance within the drug supply chain. Candidates should have at least 3 years of relevant experience and strong analytical skills. The position offers a competitive salary and benefits including PTO, life insurance, and STD/LTD coverage.

Benefits

PTO & Paid Holidays
Life Insurance
STD / LTD

Qualifications

  • 3+ years of experience in pharmacy regulatory affairs or drug supply chain.
  • Strong knowledge of FDA regulations and state pharmacy regulations.
  • Proven ability to work collaboratively and manage multiple projects.

Responsibilities

  • Research and review statutes, laws and regulations pertaining to pharmaceuticals.
  • Lead communication with regulatory agencies and ensure compliance.
  • Stay organized and prioritize tasks effectively.

Skills

Research
Analytical Skills
Communication
Time Management
Technology Skills

Education

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

Tools

Microsoft Word
Google Drive

Job description

LighthouseAI, a Pharma Solutions company, 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 will create a stress-free and streamlined state licensing experience with support from our expert industry veterans and professional solutions.

LighthouseAI - Pharmaceutical Senior Legal Research Associate

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
  • Life Insurance
  • STD / LTD

PI270893056

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