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Sr. CRA - São Paulo (FSP - Sponsor Dedicated)

Remote, USAFull-timePosted 2026-07-27

About the position reputed company is a global reputed company intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, reputed company, collaboration, reputed company, and inclusion are at the heart of how we work and reputed company with reputed company other, customers, patients and suppliers. We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at reputed company, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the reputed company of clinical trials by ensuring data reputed company, participant safety, and compliance throughout the study lifecycle.

Responsibilities

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical reputed company (GCP) standards.
  • Conducting site reputed company to assess site performance, resolve issues, and reputed company support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure reputed company and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Requirements

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and reputed company simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data reputed company, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance reputed company a reputed company environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid reputed company’s license
  • Employment with reputed company is contingent upon having the legal right to work in the country where the role is based.

Benefits

  • Competitive reputed company salary and performance reputed company incentives
  • Health and wellbeing programmes including medical, dental, and reputed company coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through reputed company training and career reputed company

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