Job Search and Career Advice Platform

Ativa os alertas de emprego por e-mail!

Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences

Teletrabalho

BRL 80.000 - 120.000

Tempo integral

Há 4 dias
Torna-te num dos primeiros candidatos

Cria um currículo personalizado em poucos minutos

Consegue uma entrevista e ganha mais. Sabe mais

Resumo da oferta

A leading life sciences recruitment firm is seeking an experienced Clinical Project Manager to oversee remote clinical projects in Brazil. The role requires at least 3 years of cross-functional PM experience with a strong focus on regulatory compliance and stakeholder communication. You will be responsible for ensuring project delivery within scope and budget, leading teams, and managing risks. This is a remote position with a 12-month duration, starting December 2025 and requiring 4 workdays per week.

Qualificações

  • Minimum 3 years of cross-functional clinical project management experience.
  • Strong understanding of regulatory GxP and RA requirements.
  • Ability to develop and deliver study plans effectively.

Responsabilidades

  • Ensure regulatory compliance and implement protocols.
  • Plan and execute clinical projects within budget and timelines.
  • Lead cross-functional teams and communicate with stakeholders.

Conhecimentos

Cross-functional clinical project management
Regulatory compliance knowledge
Stakeholder communication
Risk management

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

Obtém a tua avaliação gratuita e confidencial do currículo.
ou arrasta um ficheiro em formato PDF, DOC, DOCX, ODT ou PAGES até 5 MB.