Clinical Trial Coordinator
Core
Provide administrative and technical support to the Project Team for clinical trials, ensuring audit readiness and file reviews.
Role type
Clinical Trial Coordinator
Builds
Clinical trial documentation and regulatory compliance for commercial and government contracts
Domain
Life Sciences / Clinical Research
Required skills
Life Science degree, Organizational skills, Attention to detail, Data analysis, Customer focus, Regulatory knowledge (ICH GCP, Country Regulations), English and Turkish language skills, MS Office proficiency, Clinical trial database systems knowledge
Preferred skills
None stated
Technologies
GoBalto, eTMF, MS Office (Word, Excel, PowerPoint)
Responsibilities
Coordinate and complete functions on assigned trials activities, Perform department and Investigator file reviews, Ensure tasks are performed on time and within budget, Maintain study specific documentation and systems, Provide system support for GoBalto and eTMF, Support RBM activities, Process documents for Client (e)TMF, Schedule client and internal meetings, Review and track local regulatory documents, Transmit documents to client and IRB/IEC, Analyze and reconcile study metrics, Maintain vendor trackers, Assist with coordination of Investigator Site File and Pharmacy binder materials, Assist with study-specific translation materials and QC
Seniority
Individual Contributor