Clinical Trials Site Coordinator

Medex Smo; Zonguldak Merkez; On-site; TRY 40,000 - 60,000; Full time

Benefits offered by this job

Certification opportunities

Workshops in clinical research

Great team environment

Job summary

A clinical research organization in Turkey is seeking a Site Coordinator responsible for managing clinical trial activities under a Principal Investigator's supervision. This role involves ensuring compliance with protocols, facilitating communication among stakeholders, and overseeing volunteer safety. Ideal candidates should have a bachelor’s degree, knowledge of Good Clinical Practice (GCP), and strong organizational skills. The position offers opportunities for meaningful contributions to healthcare and collaboration with industry professionals.

Qualifications

• Bachelor's degree required.
• Knowledge of Good Clinical Practice (GCP) and regulatory requirements necessary.
• Intermediate English proficiency needed.
• Strong organizational and multitasking skills.

Responsibilities

• Manage daily activities of clinical trials.
• Facilitate communication between stakeholders.
• Ensure compliance with study protocols.
• Monitor volunteer safety and data collection.

Skills

Information about regulatory requirements

Ability to manage time effectively

Intermediate level English

Ability to handle sensitive information

Education

Minimum of a bachelor’s degree

Job description

A clinical research organization in Turkey is seeking a Site Coordinator responsible for managing clinical trial activities under a Principal Investigator's supervision. This role involves ensuring compliance with protocols, facilitating communication among stakeholders, and overseeing volunteer safety. Ideal candidates should have a bachelor’s degree, knowledge of Good Clinical Practice (GCP), and strong organizational skills. The position offers opportunities for meaningful contributions to healthcare and collaboration with industry professionals.