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.
Our benefits are designed to be competitive within each country and are 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 setup and monitoring
maintaining study documentation
patient safety compliance
Nice-to-have
foster an inclusive environment
driving innovation and excellence
strong collaborative relationships
work life balance opportunities
Key Requirements
University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines
Excellent written and verbal communication in English