PSI is a leading Contract Research Organization with more than 22 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. 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.
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, University degree in Life Sciences / Pharmacy or an equivalent combination of education, training & experience Recent on-
site monitoring experience in Russia Sufficient experience in all types of monitoring visits in Phase II and / or III Full working proficiency in English and Russian PC skills to be able to work with MS Word, Excel and PowerPoint Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-
solving skills Ability to travel Additional information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.