Clinical Research Associate II

Location: Istanbul, Turkey

Company

hirify.global develops innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Monitor clinical investigative sites for Phase 1–4 studies and ensure protocol-level execution.
• Conduct site qualification, initiation, interim monitoring, and study closeout visits.
• Identify site issues, implement corrective action plans, and maintain regulatory inspection readiness.
• Ensure data quality, timely data submission, and appropriate safety-event reporting.
• Train site personnel on study protocols and regulatory requirements.
• Manage investigator payments, negotiate investigator and hospital agreements, and identify potential investigators and sites.

Requirements

• Bachelor’s degree in a scientific or related field.
• At least 1 year of clinically related experience, including preferably 6 months in clinical research monitoring.
• Required experience conducting on-site monitoring of investigational drug or device trials.
• Fluent English, written and verbal.
• In-depth knowledge of clinical research regulations, ICH/GCP Guidelines, therapeutic indications, and applicable standard operating procedures.
• Strong planning, analytical, communication, organizational, and problem-solving skills, with demonstrated business ethics and integrity.

Culture & Benefits

• Work in a research-focused pharmaceutical environment developing medicines for serious health issues.
• Collaborate with clinical study teams, investigators, hospitals, and site personnel.
• Operate in a dynamic environment with competing projects and deadlines.
• Equal opportunity employment and a commitment to integrity, innovation, and community service.