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 and GxP requirements while managing and executing clinical projects. The position requires strong communication skills to interact with cross‑functional teams and stakeholders. Candidates should possess significant experience in clinical project management and be adaptable to evolving regulatory environments. This role is remote, starting in December 2025 for a duration of 12 months, working four days a week.

Qualificações

• 3+ years cross‑functional clinical PM experience.
• Strong understanding of regulatory and GEP requirements.
• Proficient in protocol interpretation across regions.
• Experience in end‑to‑end project delivery.

Responsabilidades

• Ensure regulatory and GxP compliance.
• Plan, execute, and close clinical projects within budget.
• Lead cross‑functional teams and foster collaboration.
• Communicate with sponsors, vendors, and stakeholders effectively.

Conhecimentos

Cross‑functional clinical project management

Regulatory knowledge

Stakeholder communication

Risk management

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