As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data
Job Summary
As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.
Skills & Requirements
Must-have
overseeing and coordinating clinical trials
ensuring compliance with regulations
collecting and analyzing critical data
study status reports and documentation
patient safety compliance
Nice-to-have
foster an inclusive environment
driving innovation and excellence
collaborative relationships with stakeholders
work life balance opportunities
Key Requirements
University degree in medicine, science, or equivalent