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 an experienced Clinical Project Manager for a remote role. Responsibilities include leading cross-functional teams, ensuring regulatory compliance, and managing clinical project timelines within budget. The ideal candidate has over 3 years of project management experience, a strong understanding of regulatory requirements, and excellent stakeholder communication skills. The position is set to start in December 2025 and requires a commitment of 4 days per week.

Qualificações

• 3+ years cross-functional clinical project management experience.
• Strong understanding of regulatory and GxP/GEP requirements.
• Proficient in developing study plans and project timelines.

Responsabilidades

• Ensure regulatory compliance and protocol implementation.
• Plan and manage clinical projects within defined scope, time, and budget.
• Lead cross-functional teams and facilitate collaboration.

Conhecimentos

Cross-functional clinical project management

Regulatory compliance knowledge

Clear stakeholder communication

Risk management

Budget forecasting

Adaptability to changes

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