Senior Clinical Trials Site Coordinator (Onsite - Kayseri)

Medex Smo; Melikgazi; On-site; TRY 30,000 - 40,000; Full time

Benefits offered by this job

Meaningful contribution to healthcare

Great team culture

Collaboration with professionals

Job summary

Medex Smo is looking for a Site Coordinator in Kayseri, responsible for managing clinical trials under the Principal Investigator's guidance. This role involves coordinating activities, ensuring compliance with GCP, and facilitating communication among stakeholders.

The ideal candidate will have at least a bachelor’s degree, knowledge of regulatory requirements, and must have proven experience in clinical studies. Join a team that values meaningful contributions to healthcare.

Qualifications

• Minimum of a bachelor’s degree.
• Knowledge of regulatory requirements and Good Clinical Practice (GCP).
• At least intermediate level English proficiency.
• At least 1 year of experience in clinical studies.

Responsibilities

• Manage clinical trials under supervision of the Principal Investigator.
• Facilitate communication between stakeholders.
• Ensure compliance with study protocols and regulatory requirements.
• Organize and monitor volunteer appointments.

Skills

Clinical studies experience

Regulatory requirements knowledge

Effective time management

Interpersonal communication skills

Ability to handle sensitive information

English proficiency (intermediate)

Education

Bachelor’s degree or higher

Job description

Medex Smo is looking for a Site Coordinator in Kayseri, responsible for managing clinical trials under the Principal Investigator's guidance. This role involves coordinating activities, ensuring compliance with GCP, and facilitating communication among stakeholders.

The ideal candidate will have at least a bachelor’s degree, knowledge of regulatory requirements, and must have proven experience in clinical studies. Join a team that values meaningful contributions to healthcare.