Job Description
We are seeking a skilled Clinical Research Associate II to provide critical support to our study sites and clinical project teams.
Key Responsibilities:
* Ensure patient safety is protected through effective site management.
* Provide guidance on audit readiness standards and support preparation for audits.
* Update and maintain trial management tools and status reports.
Requirements and Qualifications
The ideal candidate will possess a Bachelor's degree in a related field and at least 2 years of on-site monitoring experience.
Essential Skills:
* Proficiency in Microsoft Office.
* Excellent organizational skills and ability to work efficiently remotely.
About This Role
This position offers the opportunity to make a meaningful contribution to the success of our clinical research studies. If you have a passion for delivering high-quality results, we encourage you to apply.