Job Opportunity:
Oncology clinical trial monitoring demands a highly organized and detail-oriented professional to ensure the proper conduct of clinical trials in accordance with study monitoring plans and applicable laws.
Key Responsibilities:
* Clinical Trial Monitoring: Ensure the correct implementation of clinical trials in compliance with study monitoring plans and relevant regulations
* Manage operational aspects for the execution of clinical trial activities at assigned investigator sites
* Serve as the primary point of contact for assigned investigator sites, interfacing with study teams and vendors
Requirements:
* Bachelor's degree in life sciences or a professional degree in life sciences such as nursing, pharmacy, medical background, or equivalent
* Familiarity with clinical trial methodologies, ICH/GCP, FDA, and local country regulations
* A minimum of 2 years of relevant experience in clinical research site monitoring and management
* Global clinical trial experience is beneficial
* Proficiency in English and native language(s) of the country