Clinical Research Coordinator - Barcelona, Spain
On-siteMadrid, Madrid, Spain
Job Summary
Support clinical research studies and maintain a safe study environment under the direction of the Principal Investigator. Safeguard subject well-being by acting as a volunteer advocate and addressing concerns. Maintain up-to-date study protocols, case report forms, Electronic Data Capture systems, and other study documents. Plan and coordinate logistical activity for study procedures, including clinical set-up, specimen collection tube labeling, and equipment troubleshooting. Assist with data entry, quality checking, and query resolution to ensure adherence to protocol. Correctly coordinate study drug custody and respond to monitor-initiated questions. This 24-hour-per-week, 6-month contract role is based in Barcelona for a pivotal member of the site team.
Required Qualifications
- BS/BA in life sciences or educational equivalent
- relevant work experience in a clinical environment or medical setting
- Basic knowledge of clinical trials
- in-depth knowledge of departmental, protocol and study-specific operating procedures
- knowledge of consent forms
- knowledge of study schedules
- Strong IT competence
- skilled in using MS Windows
- skilled in using 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 client
- Good organizational skills with the ability to pay close attention to detail
- 24 hours per week
- 6-month contract
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