Clinical Research Associate II

PSI CRO AG · Ankara, Turkey · full-time · Hybrid · September 15, 2026

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Posted September 15, 2026 · Read from PSI CRO
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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.

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.

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

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.

Employer
PSI CRO AG
Location
Ankara, Turkey · Hybrid
Contract
full-time