
Site Management Associate I
- Ankara
- Sürekli
- Tam zamanlı
- Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team
- Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies
- Assists with handling administrative financial tasks
- Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections
- Exchanges data, documents, and other information with the project team and other departments
- Provides assistance with organization of internal team meetings
- Prepares draft minutes of internal team meetings
- Assists with preparation, attendance and follow-up of Investigator’s Meetings, as applicable
- Under supervision, maintains study-specific and corporate tracking systems
- Maintains Trial Master File (TMF)
- Perform TMF review and oversight at country and site level
- Prepares, distributes, and updates Onsite Study Files (OSF) and OSF checklists
- Provides assistance with translations
- Ensures proper safety information flow with investigative sites
- Provides miscellaneous administrative project support (if applicable)
- College/University Degree in Life Sciences
- Experience in Clinical Research / CRO environment, preferably in an international setting, is a plus
- Prior experience of work as a Site Coordinator is a plus
- Proficiency in standard MS Office applications
- Full working proficiency in English and Turkish
- Good organizational and planning skills, problem-solving abilities, flexibility
- Detail-oriented, able to multi-task and work effectively in a fast-paced environment
- Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects