Clinical Trials Site Coordinator: Efficient Study Ops

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

Benefits offered by this job

Meaningful contribution to healthcare

Great team culture

Collaboration with professionals

Job summary

A clinical trials organization seeks a Site Coordinator in Sivas Merkez, Turkey, to manage clinical trials and ensure adherence to study protocols. Responsibilities include volunteer management, facilitating communication among stakeholders, and ensuring data security and compliance with regulatory guidelines. Candidates should hold at least a bachelor's degree, have knowledge of Good Clinical Practice, and possess strong time management skills. Opportunities for professional growth in clinical research are offered.

Qualifications

• A minimum of a bachelor’s degree in a relevant field is required.
• Knowledge about regulatory requirements and Good Clinical Practice (GCP) guidelines.
• Intermediate level of English for effective communication.

Responsibilities

• Manage clinical trial activities and ensure compliance with protocols.
• Facilitate communication between various stakeholders.
• Organize volunteer appointments and support trial procedures.

Skills

Bachelor's degree

Knowledge of GCP guidelines

Intermediate English

Time management

Ethical information handling

Education

Bachelor's degree or higher

Job description

A clinical trials organization seeks a Site Coordinator in Sivas Merkez, Turkey, to manage clinical trials and ensure adherence to study protocols. Responsibilities include volunteer management, facilitating communication among stakeholders, and ensuring data security and compliance with regulatory guidelines. Candidates should hold at least a bachelor's degree, have knowledge of Good Clinical Practice, and possess strong time management skills. Opportunities for professional growth in clinical research are offered.