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
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, documenting findings accurately during site visits.
Manage information in Clinical Trial Management Systems (CTMS) and electronic Trial Master Files (eTMF), and act as a Subject Matter Expert to share best practices.
Matching 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.
Skills & Requirements
Must-have
ICH-GCP compliance
site management and monitoring
data integrity and subject safety
Clinical Trial Management Systems
regulatory documentation collection
Nice-to-have
Subject Matter Expert
continuous improvement
adaptability
accountability
Key Requirements
Bachelor’s degree
Solid experience as a Clinical Research Associate
Fluent in local languages and advanced English
Proficiency in MS Office and clinical IT applications