Study Nurse

hace 4 días

Madrid, España IQVIA A tiempo completo

Are you looking for an opportunity or a new challenge in Clinical Research? Do you want to work for an industry leading company?

IQVIA is currently recruiting for a **Research/Study Nurse **to work at our site in Madrid to support conducting a clinical trial. This part time role (24 h per week) with an immediate start is planed for **1,5 years.**

**Day to day responsibilities will include**:

- Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
- Plan and coordinate logístical activity for study procedures according to the study protocol
- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
- Assist with 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 administration and custody of study drug according to site standard operating procedures
- Collect, record, and report clinical data and findings appropriately in CRFs while collaborating with study investigator about study-related adverse events and serious adverse events according to the study protocol
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
- Bachelor's degree or educational equivalent in Nursing and one year relevant experience; or equivalent combination of education, training and experience
- 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
- 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.
- Swedish native level and good English skills

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