Clinical Research Coordinator

1 dia atrás

Brasil beBeeClinicalResearch Tempo inteiro US$45.000 - US$75.000
Job Opportunity

A Clinical Research Associate plays a key role in accelerating drug/device/outcomes research by independently monitoring studies to ensure patient safety and data integrity.

This program takes an extensive co-monitoring approach, fostering a supportive and collaborative work environment through consistent communication with clients.

Key Responsibilities

As a member of this team, you will:

  1. Conduct onsite and remote monitoring activities in compliance with ICH-GCP guidelines, applicable regulations, SOPs, and study processes.
  2. Verify informed consent procedures and protocol adherence according to applicable regulations.
  3. Maintain the integrity of clinical data and ensure the study is conducted in accordance with the approved protocol, GCP, applicable regulations, and SOPs.
  4. Oversee investigative site staff to facilitate trial deliverables, such as subject enrollment and data delivery.
  5. Ensure proper management and accountability of Investigational Product.
  6. Prepare and submit reports on investigational site findings and update relevant tracking systems.
  7. Manage essential documents required by local regulations and ICH-GCP guidelines before, during, and after the clinical study; assist with resolving investigational site/data queries.
  8. Perform risk assessments and manage responsibilities throughout the project, including risk indicator and site health analysis, process evaluation, and escalation.
  9. Participate in audit preparation and follow-up activities as needed.
  10. Carry out various onsite and offsite monitoring visits independently.
  11. Gather and review information for assigned sites, identify inconsistencies, assess risks, and escalate as appropriate with limited guidance.
Requirements

You must have:

  • An undergraduate degree or international equivalent in clinical, science, or health-related fields from an accredited institution; healthcare professional licensure (e.g., registered nurse).
  • Previous experience supporting clinical trials, including solid onsite monitoring experience.
  • Willingness to travel 50-80%.
  • Equivalent education, training, and relevant experience may be considered in place of formal education and experience. Fluency in English is required.
We Offer

In addition to a competitive salary, we provide benefits focused on well-being and work-life balance for you and your family.

Visit our careers website to learn more:

We are committed to providing an inclusive, accessible environment and a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration.

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