Remote Regulatory Licensing Specialist

LighthouseAI

United States

Remote

USD 15,940 - 19,093

Full time

14 days+

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Job summary

Triwill Group is seeking a remote Regulatory Affairs/Administrative Specialist to support the State Licensing department from Colombia. Responsibilities include drafting state pharmaceutical applications, license verification, and reviewing documents for accuracy and completeness.

The role requires 1+ year in regulatory affairs or related admin field, familiarity with licensing portals, and proficiency in Microsoft Office. Remote work with flexible hours is offered.

Qualifications

  • Minimum of one (1) year of experience in regulatory affairs, licensing, or a related administrative field.
  • Experience with regulatory data entry, application processing, or compliance documentation.
  • Familiarity with Boards of Pharmacy, DEA, or FDA is a plus.

Responsibilities

  • Draft online and hard copy state pharmaceutical applications; License verification; Review applications for accuracy.
  • Review outgoing and incoming mail and update internal database to reflect progression.
  • Maintain document repository of customer supporting documents and correspondence; perform basic Microsoft Word tasks.
  • Handle confidential information with discretion and work independently or remotely.

Skills

Regulatory affairs
Attention to detail
Communication skills

Tools

CRM software
Document management systems
Licensing portals

Job description

Triwill Group is seeking a remote Regulatory Affairs/Administrative Specialist to support the State Licensing department from Colombia. Responsibilities include drafting state pharmaceutical applications, license verification, and reviewing documents for accuracy and completeness.

The role requires 1+ year in regulatory affairs or related admin field, familiarity with licensing portals, and proficiency in Microsoft Office. Remote work with flexible hours is offered.

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