Site Operations Manager

Site Operations Manager is responsible for coordinating the operational processes of a segmentation-determined research site group, managing site teams, and ensuring effective communication with stakeholders.

This role acts as the primary and competent point of contact (Orchestrator) for central stakeholders (researchers, CROs, sponsors, hospital management, etc.) and ensures that processes are executed in alignment with institutional goals, in a measurable and transparent manner.

It offers a strategic development opportunity for professionals who wish to elevate site operations, demonstrate leadership, and exhibit ownership skills.

Saha Koordinatörü, Baş Araştırmacının gözetiminde klinik araştırmaların etkin yönetiminden ve yürütülmesinden sorumludur. Bu rol, günlük faaliyetlerin planlanmasını ve çalışma protokollerine, düzenleyici gerekliliklere ve İyi Klinik Uygulamalara (İKU) uygunluğun sağlanmasını içerir. Merkez, sponsor, iç ve dış paydaşlar arasında iletişimi kolaylaştırarak çalışma verilerinin güvenli toplanmasını, gönüllü güvenliğinin korunmasını ve düzenleyici otoritelerle uyumu sağlar.  

The Clinical Project Manager is responsible for the planning, execution, and oversight of clinical research projects. This role ensures coordination between sponsors, sites, and internal teams, while actively participating in monitoring activities and regulatory compliance. The manager ensures that project timelines, quality, and performance targets are successfully met.

The Regulatory Manager ensures that clinical trials (Phase I–IV) are conducted in compliance with local and international regulations. They manage communication with authorities such as the MoH and Ethics Committees, oversee submissions and safety reports, provide strategic regulatory guidance to project teams, ensure internal compliance, and support the development of the regulatory team.