Clinical Research Professional
hace 1 mes
We are seeking a Clinical Research Professional to join our team in Segovia, Spain. This part-time (24 hours) role is ideal for an individual looking to work in clinical research and gain valuable experience in a dynamic industry.
About the RoleThis 12-month position will provide support to the site team in conducting a clinical trial. As a pivotal member of the team, you will be involved with various administrative tasks to ensure the smooth running of clinical trials and assist with collecting patient data.
Key Responsibilities- SUPPORT CLINICAL RESEARCH STUDIES AND MAINTAIN A SAFE STUDY ENVIRONMENT ACCORDING TO HEALTH AND SAFETY POLICIES UNDER THE DIRECTION AND DELEGATION OF THE PRINCIPAL INVESTIGATOR.
- PATIENT VITAL SIGNS, ECGS, AND BLOOD WITHDRAWALS WILL BE PERFORMED BY YOU.
- Safeguard the well-being of subjects, act as a volunteer advocate, and address subjects' concerns.
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
- Plan and coordinate logistical 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 CUSTODY OF STUDY DRUG ACCORDING TO SITE STANDARD OPERATING PROCEDURES.
- COORDINATE WITH STUDY MONITOR ON STUDY ISSUES AND EFFECTIVELY RESPOND TO MONITOR-INITIATED QUESTIONS.
We are looking for candidates with a strong background in life sciences and/or relevant work experience in a clinical environment or medical setting. Ideal candidates will possess:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
- Performing patient vital signs, ECGs, and blood withdrawals.
- Basic 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.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Estimated Salary: €35,000 - €45,000 per year-
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