Pharmaceutical Senior Legal Research Associate

Lighthouseai; Philadelphia (Philadelphia County); On-site; USD 60,000 - 80,000; Full time

Job summary

Join a forward-thinking company as a Pharmaceutical Senior Legal Research Associate, where you will leverage your expertise in regulatory compliance to enhance the pharmaceutical licensing process. This full-time remote role offers the chance to research and interpret complex regulations while collaborating with a dedicated team. You'll play a pivotal role in ensuring compliance within the drug supply chain and contribute to continuous improvements in our software solutions. If you are self-motivated, detail-oriented, and passionate about the pharmaceutical industry, this opportunity is perfect for you to make a significant impact.

Qualifications

• 3-5 years of experience in researching federal and state law.
• Strong knowledge of pharmaceutical regulations like FDA regulations.

Responsibilities

• Research and interpret statutes and regulations in the pharmaceutical field.
• Lead communication with regulatory agencies and boards of pharmacy.

Skills

Research

Collaboration

Communication

Organization

Time Management

Efficiency

Technology Skills

Attention to Detail

Analytical Skills

Administrative Skills

Tools

Microsoft Word

Google Drive

Job description

Pharmaceutical Senior Legal Research Associate

About LighthouseAI
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 its clients.

Work Experience Qualifications:

• 3-5 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.