Freelance Clinical Project Manager Vaccines LATAM

K-Recruiting Life Sciences; Teletrabalho; BRL 378.000 - 488.000; Tempo integral

Resumo da oferta

A life sciences recruitment agency is seeking an experienced Clinical Project Manager in São Paulo to ensure regulatory compliance and manage clinical projects remotely. Responsibilities include leading cross-functional teams, budgeting, and stakeholder communications. Ideal candidates must have over three years of experience with a strong understanding of regulatory requirements. The role requires attendance four days per week, starting from December 2025 and lasting 12 months.

Qualificações

• 3+ years of cross‑functional clinical PM experience.
• Strong understanding of regulatory and GxP / GEP requirements.
• Proficiency in project management tools.

Responsabilidades

• Ensure compliance with regulatory requirements.
• Plan and execute clinical projects within budget.
• Oversee budget and scope change control.
• Lead cross‑functional teams for collaboration.
• Communicate with sponsors and stakeholders.
• Develop mitigation strategies for anticipated issues.

Conhecimentos

Cross‑functional clinical PM experience

Regulatory / GEP and RA / MOH knowledge

Protocol interpretation

Project delivery

Risk management

Budget forecasting

Stakeholder communication

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