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6 дней назад

Pharmaceutical Licensing Application Specialist (Colombia)

5 063 291COP
Формат работы
remote (только Colombia)
Тип работы
fulltime
Английский
c1
Страна
Colombia
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Pharmaceutical Licensing Application Specialist (Colombia) (Pharmaceutical Licensing): Preparing and managing state pharmaceutical licensing applications for clients with an accent on regulatory documentation, license verification, and application accuracy. Focus on interpreting licensing requirements, resolving board deficiencies, maintaining application records, and coordinating deadlines across multiple departments.

Location: Remote; candidates must be located in Colombia. Working hours are Monday–Friday, 8:00 a.m.–4:30 p.m. ET.

Salary: 5,063,291.14 COP per month.

Company

hirify.global provides pharmaceutical state licensing software and services, including AI-powered compliance research and licensing management tools, for manufacturers, distributors, logistics companies, and pharmacies.

What you will do

  • Draft online and hard-copy state pharmaceutical licensing applications.
  • Verify licenses and review signed applications for accuracy and completeness.
  • Review incoming and outgoing physical mail electronically while working remotely.
  • Address licensing-board deficiencies on behalf of clients and follow up on outstanding items.
  • Update internal databases and maintain repositories of applications, supporting documents, and deficiency correspondence.
  • Collaborate with Project Management, QA, the Mailroom, Accounting, clients, and licensing boards.

Requirements

  • At least one year of experience in regulatory affairs, licensing, or a related administrative field.
  • Experience with regulatory data entry, application processing, or compliance documentation.
  • Experience working in a high-volume, deadline-driven environment with strong attention to detail.
  • Advanced English proficiency equivalent to CEFR C1/C2 is required, both verbal and written.
  • Ability to interpret regulatory instructions, prepare accurate application materials, protect confidential information, and manage multiple priorities.
  • Proficiency with Microsoft Office, especially Word, Excel, and Outlook; PDF editing experience is required for administrative work.

Nice to have

  • Experience in the pharmaceutical, healthcare, or life sciences industries.
  • Familiarity with Boards of Pharmacy, DEA, or FDA.
  • Experience with document management systems, CRM software, or licensing portals.

Culture & Benefits

  • Remote work with independent and collaborative working arrangements.
  • Paid time off.
  • Paid holidays.

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