At Parexel, we share the goal of improving the world's health through clinical development solutions. The iCRA will manage and drive the strategy for startup and activation tasks of clinical studies. This role requires building relationships with investigators and ensuring compliance with local regulations and ICH-GCP guidelines
Job Summary
At Parexel, we share the goal of improving the world's health through clinical development solutions. The iCRA will manage and drive the strategy for startup and activation tasks of clinical studies. This role requires building relationships with investigators and ensuring compliance with local regulations and ICH-GCP guidelines.
Matching Summary
At Parexel, we share the goal of improving the world's health through clinical development solutions. The iCRA will manage and drive the strategy for startup and activation tasks of clinical studies. This role requires building relationships with investigators and ensuring compliance with local regulations and ICH-GCP guidelines.
Skills & Requirements
Must-have
Clinical Trial Management System (CTMS)
Informed Consent Forms (ICF)
start-up experience in clinical research
Nice-to-have
strong problem-solving skills
flexible attitude towards work
ability to work in a matrix environment
Key Requirements
degree in biological science or health-related discipline