Clinical Trials Site Coordinator - Impact & Compliance

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

Benefits offered by this job

Meaningful Contribution to Healthcare

Great team environment

Certification opportunities

Job summary

Medex Smo is seeking a dedicated Site Coordinator in Turkey’s Akdeniz Bölgesi to manage clinical trials effectively. This role involves overseeing trial activities and ensuring compliance with Good Clinical Practice (GCP) while facilitating communication among stakeholders.

Key responsibilities include screening volunteers, assisting with clinical procedures, and maintaining study data integrity. The ideal candidate holds at least a bachelor’s degree, possesses knowledge of regulatory requirements, and has strong English skills.

Qualifications

• A minimum of a bachelor’s degree.
• Information about regulatory requirements and Good Clinical Practice (GCP) guidelines.
• At least intermediate level English.
• Ability to manage time effectively and handle multiple tasks simultaneously.
• Ability to handle sensitive information ethically and professionally.

Responsibilities

• Review hospital files for preliminary volunteer screening under supervisor.
• Assist study personnel in volunteer recruitment and screening.
• Organize and monitor volunteer appointment schedules.
• Help the principal investigator perform trial procedures during visits.
• Ensure timely sending of blood samples and tracking laboratory reports.
• Assist in recording volunteer information in hospital files.
• Ensure the availability of study materials throughout the study.
• Report serious adverse events to the sponsor immediately.

Skills

Time management

Handling sensitive information

Verbal and written communication

Teamwork

Problem identification and solution development

Education

Bachelor’s degree

Master’s or PhD Degree

Job description

Medex Smo is seeking a dedicated Site Coordinator in Turkey’s Akdeniz Bölgesi to manage clinical trials effectively. This role involves overseeing trial activities and ensuring compliance with Good Clinical Practice (GCP) while facilitating communication among stakeholders.

Key responsibilities include screening volunteers, assisting with clinical procedures, and maintaining study data integrity. The ideal candidate holds at least a bachelor’s degree, possesses knowledge of regulatory requirements, and has strong English skills.