Remote Regulatory Project Manager - Global Submissions

Freyr Solutions

Bogotá ciudad

A distancia

COP 280.260.000 - 404.820.000

Jornada completa

Hace 12 días
Generador de candidaturas

Una candidatura completa en un minuto — currículum adaptado y carta de presentación, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

Flexible work options
Global exposure

Descripción de la vacante

Freyr Solutions is seeking a Regulatory Project Manager (RPM) to support global regulatory submissions and coordinate cross-functional teams in a remote, fast-paced environment. You will help plan, track, and execute campaigns across major markets, collaborating with GRT, SWG, and RRP stakeholders.

The ideal candidate has 4–6 years in pharma or life sciences, at least 2 years of project management experience, and hands-on experience with US/EU submissions.

Formación

  • Bachelor's degree in Pharmaceutical or related field.
  • 4–6 years in the pharma or life sciences industry.
  • Minimum 2 years of project management experience.
  • Experience supporting regulatory submissions for major markets (US, EU).

Responsabilidades

  • Manage SWG kick-off meetings and recurring SWG meetings.
  • Develop detailed regulatory submission timelines and RAID logs.
  • Coordinate GRT activities and RPP development.
  • Track goals, deliverables, and RAID logs for regulatory submissions.
  • Provide RPM support for non-SWG submissions.

Conocimientos

Analytical thinking
Communication skills
Multitasking
Stakeholder management
English fluency

Educación

Bachelor's degree in Pharmaceutical Sciences or related field

Herramientas

Microsoft Project
Microsoft Excel
Microsoft Word
Regulatory submission tracking

Descripción del empleo

Freyr Solutions is seeking a Regulatory Project Manager (RPM) to support global regulatory submissions and coordinate cross-functional teams in a remote, fast-paced environment. You will help plan, track, and execute campaigns across major markets, collaborating with GRT, SWG, and RRP stakeholders.

The ideal candidate has 4–6 years in pharma or life sciences, at least 2 years of project management experience, and hands-on experience with US/EU submissions.

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