Offer summary

Qualifications:

Degree in life sciences or related health profession, Strong knowledge of regulatory requirements and clinical trial processes, Fluent in English and local language (written and verbal), 2+ years of clinical on-site monitoring in interventional studies.

Key responsabilities:

Manage all phases of clinical site activity including pre-study, initiation, monitoring, and close-out visits

Ensure protocol compliance, data accuracy, patient safety, and audit readiness

Act as primary liaison with sites, vendors, and internal teams

Mentor junior staff and support project coordination as assigned

Job description

We are recruiting for our sponsor-dedicated business in Türkiye and are seeking to hire a CRA II on a permanent, full-time contract.

Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.

At Fortrea, you will have autonomy to organize your work and in return, you will be supported and empowered to go beyond the typical CRA role, to really be an expert on your protocols and to own your sites.

Summary of Responsibilities

Manage all phases of clinical site activity: pre-study, initiation, monitoring, and close-out visits
Ensure protocol compliance, data accuracy, patient safety, and audit readiness
Review source documents, resolve data queries, and oversee SAE reporting and follow-up
Act as primary liaison with sites, vendors, and internal teams
Prepare trip reports and support regulatory submissions, feasibility, and site budget negotiations
Mentor junior staff and support project coordination as assigned