Clinical Research Associate II

2 semanas atrás


São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro
Job Overview

We are seeking a skilled professional to conduct site initiation visits and monitor clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

Main Responsibilities:
  • Conduct site initiation visits and monitor clinical trials to ensure adherence to regulatory standards.
  • Coordinate data collection, including scheduling and conducting monitoring visits, reviewing and processing case report forms, and performing on-site audits.
  • Collaborate with cross-functional teams to ensure accurate and timely reporting of study results.
  • Develop strong relationships with investigators, site staff, and sponsors to facilitate effective communication and issue resolution.
Key Qualifications:
  • Bachelor's degree in a life science or related field.
  • Minimum 2 years of experience in clinical research, preferably as a clinical research associate or similar role.
  • Excellent communication and interpersonal skills, with ability to work effectively in a matrix environment.
  • Familiarity with GCP regulations, ICH guidelines, and FDA requirements.
  • Strong organizational and time management skills, with ability to prioritize multiple tasks and meet deadlines.
About the Opportunity

This is an exciting opportunity to contribute to advancing the field of clinical research. We offer a dynamic and innovative work environment, with opportunities for professional growth and development.



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