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 looking for a Clinical Project Manager to ensure regulatory compliance and oversee clinical projects. The successful candidate will have over 3 years of cross-functional PM experience, strong knowledge of RA/MOH, and skills in managing project scope, timelines, and budgets. This remote role requires clear communication with stakeholders and the ability to adapt to changes. The position starts in December 2025 and is expected to last for 12 months.

Qualificações

• 3+ years of cross-functional clinical PM experience required.
• Strong knowledge of regulatory and GEP as well as RA/MOH.
• Skills in protocol interpretation needed.

Responsabilidades

• Ensure regulatory compliance and oversight of clinical projects.
• Communicate with sponsors and manage project scope.
• Lead cross-functional teams and maintain project timelines.

Conhecimentos

Cross-functional clinical PM experience

Regulatory / GEP and RA / MOH knowledge

Protocol interpretation across regions

End-to-end project delivery

Risk, resource & milestone management

Budget forecasting

Clear stakeholder communication

Risk anticipation and 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