Clinical Research Coordinator - Bari
Support a leading company in the industry by working with our team as a Clinical Research Coordinator.
This role is for 24 hours per week and is expected to last approximately 3 months, working in Bari.
You will be responsible for supporting a clinical research study and maintaining a safe study environment according to health and safety policies under the direction of the Principal Investigator.
Key tasks include:
* Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
* Supporting screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.).
* Planning and coordinating logistical activity for study procedures according to the study protocol.
* Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
* Management and shipment of biological samples.
* Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions.
* Administrative research tasks.
We are looking for candidates with:
* A BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
* Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
* BASIC KNOWLEDGE OF MEDICAL TERMINOLOGY
* Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
* 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.
* Fluent Italian with good English language skills.
Please apply if you have the required qualifications and experience.