Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading life sciences recruiting firm is seeking an experienced Clinical Project Manager to ensure compliance with regulatory standards and manage clinical projects remotely. The ideal candidate will have at least 3 years of cross-functional project management experience and a strong understanding of regulatory and GEP requirements. The role involves oversight of budgets and timelines, stakeholder communication, and managing risks effectively. This position offers a remote work option 4 days a week with a contract duration of 12 months starting in December 2025.

Qualificações

• 3+ years of cross-functional clinical project management experience.
• Strong understanding of regulatory and GEP/RA requirements.
• Experience in protocol interpretation across regions.

Responsabilidades

• Ensure regulatory and GxP / GEP compliance.
• Plan and execute clinical projects within scope, time, and budget.
• Oversee budget forecasting and change control.

Conhecimentos

Cross-functional clinical project management

Regulatory knowledge

Risk management

Stakeholder communication

Adaptability

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