Clinical Trials Site Lead

Medex Smo; İlkadım; On-site; TRY 240,000 - 380,000; Full time

Job summary

Medex Smo is seeking a Site Coordinator to oversee the daily conduct of clinical trials under the PI. You will plan activities, ensure protocols and GCP compliance, and safeguard volunteer safety while coordinating data collection and communications with sponsors and stakeholders.

Responsibilities include screening volunteers with PI supervision, organizing visits, assisting with procedures, processing samples to labs, and maintaining accurate study records.

Qualifications

• Bachelor's degree and knowledge of regulatory requirements and GCP.
• At least intermediate level English.
• Ability to manage time effectively and handle multiple tasks.
• Ability to handle sensitive information ethically and professionally.
• At least 2 years of experience in clinical studies.

Responsibilities

• Plan daily activities and coordinate study conduct under PI supervision.
• Ensure compliance with study protocols, regulatory requirements, and GCP.
• Facilitate communication between sponsor and stakeholders; ensure data collection and volunteer safety.
• Review hospital files for preliminary volunteer screening under supervision.
• Organize and monitor appointments and volunteer visits in a timely manner.
• Prepare procedures lists and remind investigators during visits.
• Coordinate sending blood samples to labs and monitor reports.
• Record volunteer information in hospital study files.
• Ensure study materials and diaries are available throughout the study.
• Notify sponsor and monitorings of serious adverse events.

Skills

Time management

Ethical conduct

Clinical studies

English communication

Education

Bachelor's degree

Health sciences degree

Master's degree

Job description

Medex Smo is seeking a Site Coordinator to oversee the daily conduct of clinical trials under the PI. You will plan activities, ensure protocols and GCP compliance, and safeguard volunteer safety while coordinating data collection and communications with sponsors and stakeholders.

Responsibilities include screening volunteers with PI supervision, organizing visits, assisting with procedures, processing samples to labs, and maintaining accurate study records.