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Freelance Clinical Project Manager Vaccines LATAM

K-Recruiting Life Sciences

Teletrabalho

BRL 80.000 - 120.000

Tempo integral

Há 11 dias

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Resumo da oferta

A leading life sciences recruiting firm is looking for a skilled clinical project manager in Brazil for remote work. The role requires over 3 years of experience in clinical project management, strong knowledge of regulatory standards, and the ability to manage projects from planning to completion. Responsibilities include ensuring compliance with regulations, budgeting, and leading cross-functional teams to achieve project goals. This position offers 4 days of work per week for a duration of 12 months starting December 2025.

Qualificações

  • 3+ years of cross-functional clinical project management experience.
  • Strong knowledge of regulatory and GEP requirements.
  • Ability to interpret protocols across different regions.

Responsabilidades

  • Ensure compliance with regulatory and GEP standards.
  • Plan and execute clinical projects within budget and timeline.
  • Lead cross-functional teams to drive project success.

Conhecimentos

Cross-functional clinical PM experience
Regulatory knowledge
Protocol interpretation
Project delivery management
Stakeholder communication

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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