Clinical Trials Site Coordinator: Impact & Collaboration

Medex Smo; Edirne Merkez; On-site; TRY 167,400 - 279,000; Full time

Benefits offered by this job

Certification opportunities

Workshops for expertise growth

Collaborative team environment

Job summary

Medex Smo is seeking a Site Coordinator in Edirne, Turkey to effectively manage and conduct clinical trials under the supervision of the Principal Investigator. The role requires a Bachelor's Degree, knowledge of regulatory requirements, and GCP guidelines. Responsibilities include facilitating communication among stakeholders, ensuring compliance with protocols, and managing volunteer visits. A supportive team culture and certification opportunities are offered to foster professional growth.

Qualifications

• Minimum of a Bachelor’s Degree required.
• Knowledge of regulatory requirements and GCP guidelines essential.
• At least intermediate level English proficiency.

Responsibilities

• Manage and conduct clinical trials under supervision.
• Facilitate communication between sponsors and stakeholders.
• Ensure compliance with study protocols and regulations.

Skills

Time management

Handling sensitive information

Intermediate level English

Education

Bachelor’s Degree

Job description

Medex Smo is seeking a Site Coordinator in Edirne, Turkey to effectively manage and conduct clinical trials under the supervision of the Principal Investigator. The role requires a Bachelor's Degree, knowledge of regulatory requirements, and GCP guidelines. Responsibilities include facilitating communication among stakeholders, ensuring compliance with protocols, and managing volunteer visits. A supportive team culture and certification opportunities are offered to foster professional growth.