Remote Regulatory Project Manager: Global Submissions

Freyr Solutions

Bogotá ciudad

Presencial

COP 277.675.000 - 370.233.000

Jornada completa

14 días+
Generador de candidaturas

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Ventajas ofrecidas por este puesto de trabajo

Flexible work environment
Global team
Professional growth opportunities
Inclusive culture

Descripción de la vacante

Freyr Solutions is seeking a Regulatory Project Manager (RPM) Support for a remote, full-time role. You will assist in global regulatory projects, support submission activities, and coordinate cross-functional teams to meet milestones.

The role emphasizes regulatory planning, tracking, and execution of submissions, supporting Global Regulatory Teams and Submission Working Groups. Applicants should have 4–6 years in pharma or life sciences and at least 2 years of project management, with

Formación

  • Bachelor's degree in Pharmaceutical Sciences, Medical Sciences, or related scientific discipline, or equivalent experience.
  • 4–6 years of experience in pharmaceutical or life sciences industry.
  • Minimum 2 years of project management experience.
  • Experience supporting regulatory submissions for major markets (US, EU, etc.).

Responsabilidades

  • Support SWG and RAID logs, manage submission timelines.
  • Coordinate and support meetings for GRT and RPP tracking.
  • Maintain RAID logs and assist with RPM activities.
  • Independently manage non-SWG submission types.

Conocimientos

Fluency in English
Analytical thinking
Multitasking
Communication skills

Educación

Bachelor's degree in Pharmaceutical Sciences, Medical Sciences, or related field

Herramientas

Microsoft Project
Microsoft Office

Descripción del empleo

Freyr Solutions is seeking a Regulatory Project Manager (RPM) Support for a remote, full-time role. You will assist in global regulatory projects, support submission activities, and coordinate cross-functional teams to meet milestones.

The role emphasizes regulatory planning, tracking, and execution of submissions, supporting Global Regulatory Teams and Submission Working Groups. Applicants should have 4–6 years in pharma or life sciences and at least 2 years of project management, with

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