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Preparation, conduct, and reporting of all types of monitoring visits Supporting quality control, such as compliance monitoring and reports review Contact for clinical investigators, vendors and support services in regard to study progress Proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and trial supplies at sites Delivering training of investigators, site staff and project teams Be inv...
About the Role
Job Description
As a Clinical Research Associate II,you will work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
Hybrid role in Ankara, Turkey
Your responsibilities will include:
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