Freelance Clinical Project Manager Vaccines Latam

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

Resumo da oferta

A leading health recruitment firm is seeking a Remote Clinical Project Manager to oversee projects ensuring compliance with regulatory standards. The role requires expertise in managing resources, timelines, and budgets, while leading cross-functional teams effectively. Candidates must have over 3 years of experience in clinical project management, with a solid understanding of regulatory requirements. This position is part-time, requiring availability for 4 days per week, and the contract is for 12 months starting in December 2025.

Qualificações

• 3+ years of cross‑functional clinical project management experience.
• Strong understanding of regulatory requirements and protocol implementation.
• Proficient with project management tools.

Responsabilidades

• Ensure regulatory and GxP / GEP compliance.
• Plan and execute clinical projects while managing risks and resources.
• Oversee budget forecasting and scope change control.
• Lead cross‑functional teams and communicate clearly with stakeholders.

Conhecimentos

Cross‑functional clinical project management

Regulatory and GEP knowledge

Risk management

Stakeholder communication

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