Bring Your Career to Life
Job Summary:
* We are seeking a highly skilled Clinical Research Associate II to join our team.
* This role will involve monitoring clinical sites, liaising with vendors, and ensuring data integrity.
About the Role:
* The successful candidate will be responsible for all aspects of study site monitoring.
* You will work closely with vendors to ensure accurate data submission.
* Protecting study patients is a top priority, and you will verify informed consent procedures and protocol requirements.
* Quality Control Visits (QC) and Serious Adverse Event (SAE) reporting will also be part of your responsibilities.
Requirements:
* A university or college degree in a related allied health profession or certification in a relevant field.
* Demonstrated experience of at least 18 months in onsite monitoring global clinical trials.
* Familiarity with local regulatory guidelines is essential.