- Preparation conduct and reporting of selection initiation routine and closeout monitoring visits
- Site management general administration of clinical research studies in Turkey
- Contact for clinical investigators vendors and support services in regard to study progress
- Monitoring trial progress and ensuring that the project timelines are met
- Facilitation of site budgets and contract negotiations
- Effective and open communication within the project team
- Delivering training of investigators site staff and project teams
- Preparation and delivering of presentations at Investigators Meetings
- Preparation for and attendance at companys audits; resolution of audit findings
- Support to Regulatory Affairs in procurement of site regulatory documents
- Maintenance of appropriate documentation regarding clinical site management
- Participation in query resolution
Qualifications :
- University degree in Life Sciences Pharmacy or an equivalent combination of education training and experience
- Significant hands-on industry experience at a similar position with full scope of monitoring responsibilities within Phase II/III Clinical Trials
- Independent monitoring experience in Turkey and knowledge of the local clinical research environment
- Experience in regulatory submissions contract negotiations site management and feasibility assessment
- Fluent Turkish and English both spoken and written
- Team oriented with excellent communication and interpersonal skills including a positive and professional attitude to tasks and projects
- Attention to detail organizational and time-management skills
- Valid drivers license and ability to travel
Additional Information :
Take your first step towards a career in clinical research coordinating a variety of tasks and learning new things while growing with the company.
Remote Work :
Yes
Employment Type :
Full-time