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

Ontem
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 a skilled Clinical Project Manager to ensure compliance and oversee clinical projects remotely. The ideal candidate has over 3 years of cross-functional experience and a strong knowledge of regulatory requirements. You'll manage timelines, resources, and stakeholder communication, all while adapting to regulatory changes. This opportunity provides a flexible 4-days-a-week schedule, starting December 2025 with a 12-month duration.

Qualificações

  • 3+ years cross‑functional clinical PM experience.
  • Strong regulatory and RA / MOH knowledge.
  • Proficient in study plan development.

Responsabilidades

  • Ensure regulatory compliance and protocol implementation.
  • Plan, execute, and close clinical projects.
  • Lead cross-functional teams and foster collaboration.

Conhecimentos

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

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