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, including various annual leave entitlements, health insurance, competitive retirement planning, and a Global Employee Assistance Programme.
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
ICH-GCP guidelines knowledge
review and evaluate medical data
Nice-to-have
strong collaborative relationships
patient safety focus
driving innovation and excellence
fostering an inclusive environment
Key Requirements
University degree in medicine, science, or equivalent
Excellent written and verbal communication in English