Clinical Research Coordinator
hace 3 días
Job Summary:
IQVIA is seeking a highly skilled Clinical Research Coordinator / Study Nurse to support a clinical research study in a part-time role. The successful candidate will be responsible for maintaining a safe study environment, supporting the clinical trial team, and ensuring the smooth running of the clinical trial.
Key Responsibilities:
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
- Perform ECG and vital signs.
- Plan and coordinate 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.
- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
- Correct custody of study drug according to site standard operating procedures.
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
- Order and maintain study supplies.
Requirements:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
- Experience conducting ECG and taking vital signs.
- 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 Spanish and English language skills.
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