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Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences

Teletrabalho

BRL 80.000 - 120.000

Tempo integral

Hoje
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Resumo da oferta

A leading life sciences recruitment firm is seeking an experienced Clinical Project Manager to ensure regulatory compliance and manage clinical projects. Responsibilities include planning, executing, and overseeing project budgets while fostering collaboration with cross-functional teams. Candidates should have over 3 years of clinical project management experience, a strong understanding of regulatory requirements, and excellent communication skills. This remote position allows for flexible working hours, making it ideal for candidates looking to balance work and life.

Qualificações

  • 3+ years cross-functional clinical PM experience.
  • Strong regulatory and RA / MOH knowledge.
  • End-to-end project delivery and milestone management.

Responsabilidades

  • Ensure regulatory and GxP / GEP compliance.
  • Plan, execute, and close clinical projects.
  • Lead cross-functional teams and foster collaboration.

Conhecimentos

Cross-functional clinical PM experience
Regulatory knowledge
Protocol interpretation
Risk management
Stakeholder communication
Adaptability

Ferramentas

PM tools
Descrição da oferta de emprego
Tasks
  • Ensure regulatory and GxP / GEP compliance; strong understanding of RA / MOH requirements and protocol implementation across regions.
  • Plan, execute, and close clinical projects within scope, time, and budget; build timelines and manage risks, resources, and milestones.
  • Oversee budget forecasting, burn rate monitoring, and scope change control.
  • Lead cross-functional teams (Clinical, Epi, DM, Stats, Reg, PVG) and foster collaboration and accountability.
  • Communicate clearly with sponsors, vendors, and stakeholders; translate complex requirements into actionable steps.
  • Anticipate issues, develop mitigation strategies, and adapt to regulatory or operational changes.
Qualifications
  • 3+ years cross-functional clinical PM experience
  • Strong regulatory / GEP and RA / MOH knowledge
  • Protocol interpretation across regions
  • End-to-end project delivery; risk, resource & milestone management
  • Study plan development; proficient with PM tools
  • Budget forecasting, burn-rate & scope control
  • Clear stakeholder communication & actionable guidance
  • Risk anticipation, adaptability & solution-oriented approach
Requirements

Start : 12 / 2025

Duration : 12 months

Capacity : 4 days per week

Location : remote

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