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Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences

Teletrabalho

BRL 80.000 - 120.000

Tempo integral

Ontem
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Resumo da oferta

A leading life sciences recruitment firm is seeking an experienced clinical project manager to oversee regulatory compliance and manage cross-functional teams. This remote position requires over 3 years of clinical PM experience, strong knowledge of regulatory requirements, and the ability to communicate effectively with stakeholders. The role involves planning, executing, and closing clinical projects while ensuring alignment with budget and timelines. Start date is December 2025 with a capacity of 4 days per week.

Qualificações

  • 3+ years of cross-functional clinical PM experience.
  • Strong understanding of regulatory requirements.
  • Proficient in end-to-end project delivery and risk management.

Responsabilidades

  • Ensure regulatory compliance and protocol implementation.
  • Plan and execute clinical projects within scope and budget.
  • Lead cross-functional teams and foster collaboration.

Conhecimentos

Cross-functional clinical PM experience
Strong regulatory knowledge
Protocol interpretation
End-to-end project delivery
Stakeholder communication
Risk anticipation

Ferramentas

Project Management 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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