Principal Clinical Research Coordinator

1 dia atrás

São Paulo, São Paulo, Brasil beBeeClinicalTrial Tempo inteiro R$37.678 - R$59.883
Job Opportunity

We are seeking a highly skilled and experienced Clinical Trial Coordinator to join our global Clinical department.

Key Responsibilities
  • Provide administrative and technical support to the Project Team, ensuring seamless collaboration and effective communication.
  • Contribute to audit readiness by reviewing files on schedule as outlined in the organization's guidance document and departmental procedures.

The successful candidate will play a vital role in defining and developing clinical programs, minimizing delays, and executing high-quality, cost-efficient clinical studies.

Required Skills and Qualifications
  • A high school diploma or equivalent and relevant formal academic or vocational qualification.
  • Prior experience providing knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).
  • In some cases, an equivalency consisting of a combination of appropriate education, training, and/or directly related experience may be considered sufficient for an individual to meet the requirements of the role.
Benefits
  • Ability to work independently or as part of a team, demonstrating flexibility and adaptability.
  • Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.
  • Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency.
  • Strong customer focus, with excellent communication and interpersonal skills.
  • Flexibility to reprioritize workload to meet changing project timelines.
  • Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution, and closeout.
  • Good English language and grammar skills, with proficiency in local language skills as needed.
  • Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems.
  • Ability to successfully complete PPD clinical training program.
  • Self-motivation, with a proactive approach to learning and development.

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