Clinical Research Associate II

Psi CRO Ag; Çankaya; On-site; TRY 1,839,080 - 2,758,620; Full time

Job summary

Psi CRO Ag is seeking a Clinical Research Associate II to manage communication with project stakeholders and oversee clinical research projects in Ankara, Turkey. This hybrid position involves responsibilities such as monitoring visits, quality control, and supporting site regulatory processes.

The ideal candidate has a degree in Life Sciences, on-site monitoring experience, and proficiency in both Turkish and English. The role requires excellent multitasking and communication skills.

Qualifications

• 1 year of independent on-site monitoring experience.
• Native Turkish and full working proficiency in English (B2).
• Experience supporting Oncology studies is beneficial.

Responsibilities

• Preparation, conduct, and reporting of all types of monitoring visits.
• Supporting quality control, such as compliance monitoring.
• Contact for clinical investigators regarding study progress.

Skills

Monitoring visit preparation

Communication skills

Problem-solving skills

Multitasking

Education

Degree in Life Sciences

Tools

MS Office applications

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 (6 months office‑based, followed by a hybrid work model)

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
• 1 year 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.