CRA – Brazil

Planet Pharma; São Caetano do Sul; Híbrido; BRL 90 000 - 150 000; Tempo integral

Resumo da oferta

Planet Pharma is seeking an experienced Clinical Research Associate (CRA) to join our LATAM operations in Brazil, focusing on site management and monitoring for neuro-focused studies. You will oversee monitoring activities across LATAM, ensuring regulatory compliance and site performance.

The role offers a flexible hybrid work environment with travel within LATAM and potential for professional growth within a global CRO.

Qualificações

• Minimum of 2 years of independent monitoring experience, ideally 4+ years, in Brazil.
• Strong knowledge of ICH-GCP guidelines and local clinical research regulations.
• Proven site management, initiation, monitoring, and close-out experience.
• Ability to effectively manage Investigator/site relationships and documentation.
• Proactive risk identification and mitigation skills.
• Excellent communication, organizational, and problem-solving abilities.
• Fluency in English (written and verbal); Portuguese proficiency is a plus.
• Strong stakeholder management and cross-functional collaboration skills.

Responsabilidades

• Oversee site management and monitoring activities across LATAM.
• Manage multiple sites across LATAM with compliance to international standards.
• Report to Country Manager and contribute to growth in LATAM operations.

Conhecimentos

Independent monitoring

ICH-GCP knowledge

Site management

Investigator relationships

Risk mitigation

Communication

English fluency

Portuguese proficiency

Stakeholder management

Global environment adaptability

Formação académica

Bachelor’s degree in Life Sciences

Nursing or related field

Descrição da oferta de emprego

Join Our Team as a CRA - Brazil and Drive Innovation in Clinical Research!

Are you an experienced Clinical Research Associate eager to make a real impact in the fast-paced world of clinical trials? A dynamic global CRO committed to advancing healthcare through cutting-edge therapies, is seeking a dedicated CRA to join our expanding LATAM operations in São Paulo. If you thrive on collaboration, possess a proactive mindset, and want to be part of a company that values growth and professional development, this is the opportunity for you!

Role Overview

As a CRA in Brazil, you will be at the forefront of clinical research innovation, managing multiple sites across LATAM. You will oversee site management and monitoring activities for neuro-focused studies, ensuring compliance with international standards and local regulations. Reporting directly to the Country Manager, you’ll enjoy a flexible work environment with the chance to grow your skills in a truly global organization. This role offers the perfect blend of responsibility, diversity, and opportunity to accelerate your career in clinical research.

Required Skills & Qualifications

• Minimum of 2 years of independent monitoring experience, ideally 4+ years, in Brazil
• Strong knowledge of ICH-GCP guidelines and local clinical research regulations
• Proven site management, initiation, monitoring, and close-out experience
• Ability to effectively manage Investigator/site relationships and documentation
• Proactive risk identification and mitigation skills
• Excellent communication, organizational, and problem-solving abilities
• Fluency in English (written and verbal); Portugueseproficiency is a plus
• Strong stakeholder management and cross-functional collaboration skills
• Ability to thrive in a fast-paced, global environment

Nice to Have Skills

• Experience working across multiple sites in LATAM
• Prior involvement in neuro-focused studies
• Familiarity with regulatory and ethics committee interactions
• Multilingual capabilities, especially for better regional communication

Preferred Education & Experience

• Bachelor’s degree in Life Sciences, Nursing, or related fields
• 2+ years of experience in clinical site monitoring, particularly in Brazil
• Previous exposure to neuro research studies is advantageous

Other Requirements

• Location: São Paulo, Brazil
• Flexibility for work-from-home when not on-site
• Willingness to travel
• Valid clinical research certifications are preferred but not mandatory

This is your chance to join a forward-thinking organization that fosters growth, diversity, and excellence in clinical research. Accelerate your career- where innovation meets opportunity. Ready to take the next step?