Senior Clinical Research Associate

Psi CRO Ag; Çankaya; On-site; TRY 922,509 - 1,845,018; Full time

Job summary

Psi CRO Ag is seeking a Clinical Research Associate II to manage clinical research projects in Ankara, Turkey. This hybrid role involves building relationships with clinical sites and ensuring compliance with research standards.

Key responsibilities include preparing and conducting monitoring visits, supporting quality control, and delivering training to investigators and site staff. Applicants should have a degree in Life Sciences and 3 years of on-site monitoring experience. Proficiency in Turkish and English is required.

Qualifications

• 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).

Responsibilities

• Preparation, conduct, and reporting of monitoring visits.
• Supporting quality control and compliance monitoring.
• Deliver training to investigators and site staff.

Skills

Independent on-site monitoring

Communication skills

Collaboration skills

Problem-solving skills

Proficiency in MS Office

Ability to multitask

Education

Degree in Life Sciences or similar

Job description

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
• 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.