Clinical Operations Specialist

Há 7 dias

Brasil beBeeAdministrative Tempo inteiro R$2.500 - R$4.500
Job Summary

We are seeking a diligent and organized Clinical Research Associate to provide administrative support to our project team. The ideal candidate will have excellent organizational skills, strong attention to detail, and the ability to work independently or as part of a team.

Key Responsibilities
  • Provide administrative and technical support to the project team.
  • Ensure files are reviewed according to the schedule detailed in our SOP and department guidance document.
  • Aid in the development of critical paths for site activation within assigned projects.
  • Represent CRG personnel and provide local input into the site tiering process.
Qualifications

Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. Bachelor's degree preferred. Previous experience providing knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year). An equivalency consisting of a combination of appropriate education, training and/or directly related experience may also be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities: Ability to work in a team or independently as required; good organizational skills and strong attention to detail; demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency; strong customer focus; 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/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout; good English language and grammar skills and proficient 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 our clinical training program; self-motivated, positive attitude and good interpersonal skills; effective oral and written communication skills; good interpersonal skills; essential judgment and decision-making skills; capable of accurately following project work instructions; good negotiation skills; independent thinker; ability to manage risk and perform risk escalation appropriately.


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