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.
Role bases in Ankara,Türkiye
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
- 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
- Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
- 1 year and a half of independent on-site monitoring experience in Türkiye, ideally on multiple projects at a time
- Experience in all types of monitoring visits in Phase II and/or III
- Native Turkish and full working proficiency in English
- Experience supporting Oncology studies is beneficial, but not essential
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- As you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel.
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
