Site Research Assistant supporting a clinical research site in Nijmegen. Performing administrative and clinical support tasks for smooth execution of clinical trials.
Responsibilities
Help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks
Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
Coordinating logistical activities for study procedures in line with the study protocol
Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
Communicating with study monitors and responding to study-related inquiries
Help with patient recruitment, patient education and community outreach
Carrying out general administrative tasks related to the study
Requirements
Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
Good knowledge of medical terminology
Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
Excellent interpersonal and communication skills
Strong organizational skills and attention to detail
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