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.
Develop and maintain strong relationships with study sites throughout all phases of clinical trials.
Conduct remote and on-site monitoring to ensure data integrity and subject safety.
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
Clinical Trials Monitoring
Site Management
Data Integrity
Protocol Adherence
Regulatory Compliance
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 proficiency in English
Strong understanding of clinical research processes
Proven skills in site management and patient recruitment