Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences; Betim; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A dynamic life sciences recruitment firm is seeking an experienced clinical project manager to oversee regulatory compliance, manage clinical projects, and lead cross-functional teams. This role involves ensuring timelines and budgets are followed, building stakeholder relationships, and adapting to changes in regulations. Candidates should have over 3 years of experience in project management within the clinical field, along with strong knowledge of regulatory requirements. The position offers remote work 4 days a week starting in December 2025.

Qualificações

• 3+ years of cross-functional clinical project management experience.
• Strong understanding of regulatory (GEP) and RA/MOH requirements.
• Ability to interpret protocols across regions.

Responsabilidades

• Ensure regulatory and GxP/GEP compliance.
• Plan, execute, and close clinical projects within scope, time, and budget.
• Lead cross-functional teams and foster collaboration.

Conhecimentos

Cross-functional clinical project management

Regulatory knowledge (GEP, RA, MOH)

Risk and resource management

Stakeholder communication

Adaptability

Study plan development

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.

Qualification

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