Clinical Research Associate II

PSI CRO

Not Interested
Bookmark
Report This Job

profile Job Location:

Ankara - Turkey

profile Monthly Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

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 Investigators Meetings
  • Maintenance of study-specific automated tracking systems
  • Preparation for and attendance at companys 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 drivers 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.


Remote Work :

No


Employment Type :

Full-time

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 investigator...
View more view more

About Company

Company Logo

PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effo ... View more

View Profile View Profile