Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences; São Paulo; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading recruitment firm in Life Sciences is looking for an experienced Project Manager to manage clinical projects. The role involves ensuring regulatory compliance, overseeing project timelines, and communicating effectively with stakeholders. Ideal candidates should have over 3 years of cross-functional clinical PM experience and solid knowledge of regulatory standards. This position is remote, requiring four working days per week, and has a contract duration of 12 months starting on December 2025.

Qualificações

• 3+ years of cross-functional clinical project management experience.
• Strong knowledge of regulatory standards and requirements (GEP, RA).
• Ability to manage project timelines, risks, and resources.

Responsabilidades

• Ensure compliance with regulatory and GxP/GEP standards.
• Communicate clearly with sponsors and stakeholders.
• Oversee budget and scope change control.

Conhecimentos

Cross-functional clinical project management

Regulatory knowledge (GEP, RA)

Stakeholder communication

Budget forecasting

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