Clinical Research Associate II

Job Location

Saint Petersburg, Russia

Job Description

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Job Description

As a Clinical Research Associate 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.

St. Petersburg, Russia

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

Job Requirements


  • MD, College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in Russia
  • Experience in all types of monitoring visits in Phase II and/or III
  • Medical experience is a plus
  • Full working proficiency in English and Russian
  • 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.

Experience required: Associate

Click Here to Apply

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Contact Information

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January 21, 2020
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