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QIMA

Quality control, auditing, testing, and compliance

Technicien d'Etudes cliniques Intern

Clinical Support & Patient AdministrationPosted on Nov 9
Internship · Winter 2026Nice, FranceNo salary listed

About the Job

Requirements

  • Bac+3/5 in a scientific or medical domain, or Bac+2 with three years of clinical research experience.
  • Mastery of written and spoken French at B2 level.
  • Good knowledge of office tools for data entry.
  • Good comprehension of written English at B2 level.

Responsibilities

  • Manage logistics and data collection for clinical studies in compliance with regulations and deadlines at the investigator site.
  • Assist the investigator in clinical patient follow-up.
  • Participate in patient screening and recruitment, which may include a brief presentation of the preliminary study before the investigator explains it and collects consent.
  • Apply products to volunteers’ skin and take measurements.
  • Prepare and use the equipment and measurement instruments required for trials, including adjustment and calibration.
  • Enter data in the tools implemented with the sponsor.
  • Follow up with patients by telephone and send reminders for follow-up visits.
  • Manage logistics for patients enrolled in the study, including coordinating appointments with different departments, managing treatment dispensing, organizing each patient visit, and handling laboratory samples through preparation, storage, and shipment.
  • Participate in monitoring visits by the sponsor’s clinical research associate.
  • Prepare study visits and make related documents available.
  • Manage corrections and follow-up actions with the sponsor’s clinical research associate present.
  • Resolve clarification requests from data management or the sponsor’s clinical research associate during the study.
  • Update the investigator site file.
  • Participate in investigator and/or staff meetings as needed.
  • Collect documents required for site initiation in coordination with the sponsor’s clinical research associate.
  • Organize and participate in study initiation visits.
  • Write protocol-specific procedures and technical sheets for the site team.
  • Participate in quality management system improvement.
  • Participate in writing mock reports.
  • Manage selection, qualification, monitoring, use, and maintenance of measurement instruments and biomedical equipment.
  • Manage subcontracting of human biology analyses.
  • Manage medical supplies and research consumables.
  • Participate in reviewing final reports.

Desired Qualifications

  • Very good interpersonal skills to welcome and support participants.
  • A conscientious and curious profile.

About the Company

QIMA

Quality control, auditing, testing, and compliance

QIMA provides quality control and compliance services to brands, retailers, and importers. It offers inspection, auditing, and testing to ensure product safety, supplier performance, and regulatory compliance across manufacturing facilities worldwide. The services translate into real-time supply chain intelligence that helps clients monitor and improve quality and ESG-related outcomes, with fees-based revenue supported by accreditation from regulatory bodies and international standards. Unlike firms that offer only one aspect of QA, QIMA combines multiple assurance activities with a trusted, accredited framework and simple, client-focused service to give end-to-end visibility and control over supplier performance. The company’s goal is to help clients produce trustworthy products while prioritizing client satisfaction, integrity, and simplicity in operations.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Hong Kong
Founded
2005

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