As a Senior Clinical Research Associate/ 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:
- 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 involved in site identification process and feasibility research
- Support to Regulatory Affairs in procurement of site regulatory documents
- Preparation and delivering of presentations at Investigator’s Meetings
- Maintenance of study-specific automated tracking systems
- Preparation for and attendance at company’s audits; resolution of audit findings