Log inSign up free
  • Home
  • Jobs
    • Applications
    • Career
    • Resume
    • Cover letters
  • Content
    • Posts
    • Media
  • Messages
  • Analytics
    • Overview
    • Pages
  • Builder
    • Templates
  • More tools
    • Profile
    • Hiring
  • Settings
All jobs
IQIqvia logo

Iqvia

Athens

Clinical Research Coordinator - Athens.

PART TIMEON-SITE€27.4K–41K/YR
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. We have a new part time project in Athens for up to 15-20 hours per week. It will be for 6-7 months and will support an oncology clinical trial on site in Athens. As a key member of the site team, you will play an important role in supporting investigators and helping to ensure the smooth day-to-day delivery of clinical trials. You will act as the go-to person for data entry and query resolution, while also playing an active role in patient recruitment and engagement. This is a varied position offering the opportunity to make a meaningful contribution to the successful delivery of clinical research. Day to day responsibilities will include: 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 Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s 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 the following skills and experience: BS/BA in life sciences or educational equivalent and/or relevant work experience as a clinical research coordinator At least three years of experience in oncology clinical trials Excellent 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 client Good organizational skills with the ability to pay close attention to detail. #LI-DNP #LI-CES #LI-HCPN #LI-CT1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is €27,400.00 - €41,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
Pay
€27.4k–41k/yr
Where
Athens · Greece
Work
On-site
Type
Part time
Posted
30 Oct, 2026
Apply on the original postingSign in to apply

Verified board

more at Iqvia.

2 Nov, 2026

Iqvia

Records Management Associate

IQIqvia logo

    Pasig, Philippines

    Salary not listed

    Details
    2 Nov, 2026

    Iqvia

    Young Professionales (m/w/d) - Neueinsteiger (m/w/d)

    IQIqvia logo

      Mannheim +2

      Salary not listed

      Details
      2 Nov, 2026

      Iqvia

      Neueinsteiger und erfahrene Mitarbeiter im Pharma- und Apothekenaußendienst (m/w/d) - Großraum Würzburg/Nürnberg

      IQIqvia logo

        Location not stated

        Salary not listed

        Details

        similar roles.

        29 Jul, 2026

        helloavahealth.com

        Nurse LPN Residential

        HChelloavahealth.com logo
        • Full time

        Grand Junction, Colorado

        Full time

        Details
        2 Nov, 2026

        KEYENCE FRANCE

        Coordinateur/trice administration des ventes Junior F/H

        KFKEYENCE FRANCE logo
        • Full time
        • Junior level

        Nantes, fr

        Full time

        Details
        2 Nov, 2026

        KEYENCE FRANCE

        Assistant(e) ADV junior F/H

        KFKEYENCE FRANCE logo
        • Full time
        • Junior level

        Nantes, fr

        Full time

        Details
        27 Aug, 2026

        Dialogue

        Mental Health Intake Agent, Temporary

        DIDialogue logo
        • Part time
        • Remote

        Remote (Canada)

        Remote

        Details
        29 Oct, 2026

        propharmagroup

        CEE Regulatory Affairs and Pharmacovigilance Specialist

        PRpropharmagroup logo

          Belgrade, Serbia

          Salary not listed

          Details
          29 Oct, 2026

          propharmagroup

          Pharmacovigilance Specialist, Case Processing

          PRpropharmagroup logo

            Belgrade, Serbia

            Salary not listed

            Details