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Senior Clinical Research Associate I

PSI CRO

Çankaya

On-site

TRY 80,000 - 120,000

Full time

30+ days ago

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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

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