Clinical Study Coordinator
1 settimana fa
We are looking for a Clinical Research Coordinator to work at our site in **Meldola** on an Oncology trial**. **This role is a part time role for **24h/week **and will be for **3-6 months.**
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting data.
**Day to day responsibilities will include**:
- Providing clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents,
- EDC entry and query resolution
- Maintain Study Supplies
- Upkeep Regulatory Binder
- Review Charts from Site Database
- Update Study Portals
- Attend all relevant study meetings
- Collect and submit regulatory/ethics documentation as required by relevant regulatory bodies governing the conduct of clinical research
- Design and maintain source documentation based on protocol requirements
- Schedule and execute study visits and perform study procedures
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
- Knowledge of medical terminology
- Knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
- Must have previous experience of EDC entry and query resolution
- Must have experience in Oncology
- Ability to pay close attention to detail
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
- Good organizational skills with the ability to pay close attention to detail
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