Senior Clinical Research Associate I

PSI CRO; Çankaya; On-site; TRY 80,000 - 120,000; Full time

Job summary

A leading Swiss Contract Research Organization seeks a Clinical Research Associate to manage and monitor clinical trials in Turkey. Responsibilities include site management, investigator training, and ensuring compliance with project timelines. The ideal candidate possesses a degree in Life Sciences or Pharmacy and extensive industry experience. Join PSI CRO for a progressive career in clinical research.

Qualifications

• Significant hands-on industry experience in Phase II/III Clinical Trials.
• Independent monitoring experience in Turkey.
• Fluent in Turkish and English.

Responsibilities

• Conduct and report monitoring visits.
• Manage clinical research studies in Turkey.
• Prepare for company audits.

Skills

Communication

Interpersonal Skills

Attention to Detail

Organizational Skills

Time-management

Education

University degree in Life Sciences or Pharmacy

Job description

Company Description

PSI is a leading Swiss Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

• Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
• Site management, general administration of clinical research studies in Turkey
• Contact for clinical investigators, vendors and support services in regard to study progress
• Monitoring trial progress and ensuring that the project timelines are met
• Facilitation of site budgets and contract negotiations
• Effective and open communication within the project team
• Delivering training of investigators, site staff and project teams
• Preparation and delivering of presentations at Investigator’s Meetings
• Preparation for and attendance at company’s audits; resolution of audit findings
• Support to Regulatory Affairs in procurement of site regulatory documents
• Maintenance of appropriate documentation regarding clinical site management
• Participation in query resolution

Qualifications

• University degree in Life Sciences, Pharmacy,or an equivalent combination of education, training and experience
• Significant hands-on industry experience at a similar position, with full scope of monitoring responsibilities within Phase II/III Clinical Trials
• Independent monitoring experience in Turkeyand knowledge of the local clinical research environment
• Experience in regulatory submissions, contract negotiations, site management and feasibility assessment
• Fluent Turkishand English, both spoken and written
• Team oriented with excellent communication and interpersonal skills including a positive and professional attitude to tasks and projects
• Attention to detail, organizational and time-management skills
• Valid driver’s license and ability to travel

Additional Information

Take your first step towards a career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.