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Clinical Research Coordinator

Apsida Life Science · Adana

New
Contrat Onsite 🇬🇧 English
ICH-GCP

Job description

About the role

The Clinical Research Coordinator will support and manage oncology clinical trial activities across multiple sites in Turkey, ensuring compliance with protocols and regulations.

Key responsibilities

  • Coordinate and support clinical trial activities at assigned sites.
  • Work closely with investigators, site staff, sponsors, and other study stakeholders.
  • Support patient visits and study procedures in accordance with the study protocol.
  • Maintain accurate and timely study documentation and records.
  • Assist with study start‑up, ongoing activities, and close‑out as required.
  • Ensure activities comply with GCP, SOPs, and applicable regulations.
  • Support monitoring visits, audits, and inspections.

Required profile

  • Previous experience as a Clinical Research Coordinator or Study Coordinator.
  • Experience working within clinical trials, preferably in oncology.
  • Understanding of ICH‑GCP and clinical trial requirements.
  • Strong organizational and communication skills.
  • Ability to work independently while collaborating with site and study teams.
  • Willingness to provide on‑site support as required.

Questions fréquentes

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Le contrat proposé est un Contrat basé à Adana.

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Published 4 hours ago

Expires 1 month from now

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Apsida Life Science

Adana

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