Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences; Teletrabalho; BRL 381.000 - 490.000; Tempo integral

Resumo da oferta

A leading life sciences recruitment firm is looking for a remote Clinical Project Manager in Brazil. The role requires 3+ years of cross‑functional clinical project management experience and strong regulatory knowledge. Responsibilities include ensuring regulatory compliance, planning and executing projects, overseeing budgets, and leading cross-functional teams. This position is for 12 months, starting in December 2025, requiring a capacity of 4 days per week. Competitive compensation will be provided.

Qualificações

• 3+ years of cross‑functional clinical project management experience.
• Strong knowledge of regulatory and GxP requirements.
• Proficient in project management tools.

Responsabilidades

• Ensure regulatory compliance and protocol implementation.
• Plan, execute, and close clinical projects.
• Oversee budget forecasting and change control.
• Lead cross‑functional teams and foster collaboration.
• Communicate with sponsors and stakeholders.
• Anticipate issues and develop mitigation strategies.

Conhecimentos

Cross‑functional clinical project management

Regulatory and GxP knowledge

Protocol interpretation

End‑to‑end project delivery

Budget forecasting

Stakeholder communication

Risk management

Adaptability

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