leHACK is seeking a Clinical Research Associate II to oversee clinical trials in São Paulo or Porto Alegre, Brazil, ensuring compliance and effective site management. The ideal candidate should possess solid experience in clinical research, excellent communication skills, and the ability to manage multiple tasks in a fast-paced environment
Job Summary
You will be the primary site contact throughout all phases of clinical research studies, ensuring compliance with regulations and contributing to the success of our clinical trials.
Conduct remote and on-site monitoring to ensure data integrity and subject safety.
Manage information in Clinical Trial Management Systems (CTMS) and electronic Trial Master Files (eTMF).
Matching Summary
Match Score: 85
leHACK is seeking a Clinical Research Associate II to oversee clinical trials in São Paulo or Porto Alegre, Brazil, ensuring compliance and effective site management. The ideal candidate should possess solid experience in clinical research, excellent communication skills, and the ability to manage multiple tasks in a fast-paced environment.
Skills & Requirements
Must-have
ICH-GCP compliance
site management and monitoring
protocol adherence
data integrity
subject safety
regulatory documentation review
Nice-to-have
strong relationships with study sites
continuous improvement of processes
Subject Matter Expert
best practices sharing
training provision
Key Requirements
Bachelor’s degree
Solid experience as a Clinical Research Associate
Fluent in local languages
advanced proficiency in English
Proficiency in MS Office and clinical IT applications