Clinical Trials Site Coordinator — Certification & Impact

Medex Smo; Konak; On-site; TRY 30,000 - 50,000; Full time

Benefits offered by this job

Certification opportunities

Workshops to grow expertise in clinical research

Job summary

Medex Smo seeks a Site Coordinator in Turkey, Ege Bölgesi, Konak, responsible for managing clinical trials and ensuring compliance with regulatory requirements. The ideal candidate should have at least a bachelor's degree, intermediate English proficiency, and knowledge of GCP guidelines. This role involves coordinating activities, maintaining safety protocols, and ensuring effective communication between all stakeholders. The position offers opportunities for professional growth in clinical research.

Qualifications

• Minimum of a bachelor’s degree required.
• Intermediate English proficiency.
• Knowledge of GCP guidelines and regulatory requirements.
• Ability to manage multiple tasks simultaneously.

Responsibilities

• Manage and conduct clinical trials under supervision.
• Ensure compliance with study protocols and GCP.
• Facilitate communication with stakeholders.
• Track and report serious adverse events.

Skills

Information about regulatory requirements and GCP guidelines

Ability to manage time effectively

Ability to handle sensitive information ethically

Intermediate level English

Education

Bachelor's degree

Job description

Medex Smo seeks a Site Coordinator in Turkey, Ege Bölgesi, Konak, responsible for managing clinical trials and ensuring compliance with regulatory requirements. The ideal candidate should have at least a bachelor's degree, intermediate English proficiency, and knowledge of GCP guidelines. This role involves coordinating activities, maintaining safety protocols, and ensuring effective communication between all stakeholders. The position offers opportunities for professional growth in clinical research.