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PSI CRO

200 open roles · Clinical

Clinical Research Associate II / Senior CRA

Full-time
Senior
Posted 1 month ago
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Where you can work

Hybrid

Kyiv, Kyiv City, Ukraine

View location wording from the posting
Kyiv, Kyiv city, Ukraine

Role overview

Extracted from the posting. Read the employer’s full description below.

What they are looking for

  • MD, PharmD or MSc
  • 2+ years of independent on-site monitoring experience in Ukraine
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology/Ulcerative Colitis/Antibiotics trials is a plus
  • Full working proficiency in English and Ukrainian
Show all 9 items
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Employer description

Company Description

PSI is a leading 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

As a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Hybrid role in Kyiv, Ukraine

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions

Qualifications

  • MD, PharmD or MSc
  • 2+ years of independent on-site monitoring experience in Ukraine
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology/Ulcerative Colitis/Antibiotics trials is a plus
  • Full working proficiency in English and Ukrainian
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • 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.

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Source: SmartRecruiters