Clinical Trials Site Coordinator: Impactful Coordination

Medex Smo; Seyhan; On-site; TRY 180,000 - 300,000; Full time

Benefits offered by this job

Certification opportunities

Workshops for expertise growth

Collaborative work environment

Job summary

A healthcare organization seeks a Site Coordinator to manage clinical trials in Turkey. Responsibilities include ensuring compliance with regulations, managing communications between stakeholders, and overseeing volunteer safety. The ideal candidate will have a bachelor's degree, knowledge of GCP guidelines, and effective time management skills. This role offers opportunities for professional growth, teamwork, and making a meaningful contribution to healthcare.

Qualifications

• Minimum of a bachelor's degree required.
• Knowledge of regulatory requirements and GCP guidelines.
• At least intermediate English proficiency.

Responsibilities

• Manage clinical trials under supervision of Principal Investigator.
• Facilitate communication among sponsors and stakeholders.
• Ensure compliance with study protocols and regulatory requirements.

Skills

Time management

Ethical handling of sensitive information

Intermediate level English

Strong teamwork

Excellent verbal and written communication skills

Education

Bachelor's degree

Job description

A healthcare organization seeks a Site Coordinator to manage clinical trials in Turkey. Responsibilities include ensuring compliance with regulations, managing communications between stakeholders, and overseeing volunteer safety. The ideal candidate will have a bachelor's degree, knowledge of GCP guidelines, and effective time management skills. This role offers opportunities for professional growth, teamwork, and making a meaningful contribution to healthcare.