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 Senior CRA 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.
You will :
Conduct and report all types of onsite monitoring visits
Perform CRF review, source document verification and query resolution
Be responsible for site communication and management
Supervise study activities, timelines, and schedules on the country level
Be a point of contact for in-house support services and vendors
Be involved in quality control, such as compliance monitoring and reports review
Participate in feasibility research
Support regulatory team in preparing documents for study submissions
MD, PharmD, University degree in Life Sciences or an equivalent combination of education, training & experience
Independent on-site monitoring experience in Ukraine
Experience in all types of monitoring visits in Phase II and / or III
Participation in clinical projects as a Lead / Senior Monitor
Experience in Asthma / Ulcerative Colitis / MS / antibiotics / oncology trials is a big 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
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.