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 recruitment firm is seeking a remote Clinical Project Manager to ensure regulatory compliance and manage clinical projects. You will oversee project timelines, collaborate with cross-functional teams, and communicate with stakeholders. The ideal candidate has over 3 years of clinical project management experience and a strong understanding of regulatory requirements. This position offers a flexible capacity of 4 days per week for 12 months, starting in December 2025.

Qualificações

• 3+ years of cross-functional clinical project management experience.
• Strong knowledge in regulatory compliance and RA/MOH requirements.
• Experience in protocol interpretation across different regions.
• Proficient in project delivery and risk management.

Responsabilidades

• Ensure regulatory and GxP/GEP compliance for clinical projects.
• Plan and execute clinical projects while managing timelines and resources.
• Lead cross-functional teams to foster collaboration.

Conhecimentos

Clinical project management

Regulatory compliance

Stakeholder communication

Risk management

Budget forecasting

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