
Clinical Research Coordinator
IQVIA
part-time
Posted on:
Location Type: Office
Location: Toledo • Spain
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About the role
- 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
- Supporting patient screening and enrollment, including handling informed consent and privacy documentation
- 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
- Managing and shipping biological samples
- 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
- Fluency in Spanish and good command of English.
Benefits
- Supportive work environment
- Impactful projects
- Opportunity to make a real difference
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
data entryquality checksclinical trial executionstudy documentation maintenancepatient screeninginformed consent handlingbiological sample managementmedical terminology knowledgeclinical research coordinationpatient recruitment
Soft Skills
interpersonal skillscommunication skillsorganizational skillsattention to detail