IQVIA

Clinical Research Coordinator

IQVIA

part-time

Posted on:

Location Type: Office

Location: ToledoSpain

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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