Site Research Assistant
IQVIA
part-time
Posted on:
Location Type: Office
Location: Strasbourg • 🇫🇷 France
Visit company websiteJob Level
JuniorMid-Level
About the role
- Supporting a clinical research study and maintaining a safe study environment
- Involved with a variety of administrative tasks to support the clinical trial team
- Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems
- Support with screening and enrollment of patients
- Planning and coordinating logistical activity for study procedures
- Data entry, data quality checking, and query resolution
- Management and shipment of biological samples
- Coordinating with study monitor on study issues
Requirements
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment
- Good knowledge of clinical trials
- Must have at least 1-2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator
- 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
- Good organizational skills
Benefits
- Health and safety policies
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data entrydata quality checkingquery resolutioncase report formsElectronic Data Capturebiological sample managementclinical trial supportpatient screeningpatient enrollmentstudy protocol maintenance
Soft skills
interpersonal skillsorganizational skills