Clinical Research Associate II

PSI CRO·Ankara, Ankara, Türkiye

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About the role

Hybrid Clinical Research Associate II role in Ankara, Türkiye, supporting Phase II and/or III clinical studies. Responsibilities include monitoring visits, site and investigator coordination, quality and compliance activities, investigational product accountability, training, feasibility, regulatory document support, tracking systems, and audit follow-up. Requires 2–3 years of independent on-site monitoring experience, Turkish and English proficiency, and a valid driver’s license with travel ability.

Key requirements

• Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
• At least 2 years of relevant experience
• Required skills: Independent on-site monitoring, Monitoring visits in Phase II and/or III studies, Clinical site and investigator relationship management, Quality control and compliance monitoring, Investigational product and trial supply accountability, Investigator and site staff training, Site identification and feasibility research, Regulatory document procurement support, Study-specific tracking systems, Audit preparation and finding resolution, MS Office, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
• Required languages: Turkish, English
• Professional registration/licence (Türkiye)

Opportunity details

• Workplace: Hybrid
• Employment: Permanent
• Posted: Sep 15, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Clinical Research Associate II

Location: Ankara, Ankara, Türkiye

Employment type: Full-time

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Hybrid role in Ankara, Turkey

Your responsibilities will include:

Preparation, conduct, and reporting of all types of monitoring visits
Supporting quality control, such as compliance monitoring and reports review
Contact for clinical investigators, vendors and support services in regard to study progress
Proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and trial supplies at sites
Delivering training of investigators, site staff and project teams
Be involved in site identification process and feasibility research
Support to Regulatory Affairs in procurement of site regulatory documents
Preparation and delivering of presentations at Investigator’s Meetings
Maintenance of study-specific automated tracking systems
Preparation for and attendance at company’s audits; resolution of audit findings

Qualifications

Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
2-3 years of independent on-site monitoring experience
Experience in all types of monitoring visits in Phase II and/or III
Native Turkish and full working proficiency in English (B2)
Experience supporting Oncology studies is beneficial, but not essential
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
As you will be monitoring multiple sites, you must have a valid driver's license, and the ability to travel.

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.