Clinical Research Associate / Senior CRA
Posted 9 days agoConfirmed open 35 min ago
Who can apply
Ukraine only
Salary
Not disclosed
Level
Entry level
Full-time
Timezone
Not stated
About the role
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. You will be collaborating with experienced clinical research professionals who are committed to quality, teamwork, and advancing clinical research.
Remote role in Ukraine
Your responsibilities will include:
- Preparing, conducting, and reporting on all types of monitoring visits, including site selection, initiation, routine monitoring, and close-out visits
- Ensuring compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
- Building and maintaining strong relationships with investigators and site staff
- Monitoring patient recruitment, study timelines, and site performance
- Performing source data verification, following up on data queries, and managing site-level risks
- Overseeing investigational product accountability, trial supplies, and essential study documentation
- Maintaining Investigator Site Files (ISF) and supporting Trial Master File (TMF) reconciliation
- Delivering study-specific training to investigators and site staff
- Supporting regulatory submissions, audit preparation, and resolution of audit findings
Qualifications
- MD, PharmD or MSc
- 1+ year 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.
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.
Skills mentioned
Interested in this role?
You apply directly with PSI CRO. Remotavia never charges candidates.
Check your resume
See which keywords from this job your resume is missing.
Track this application
Add it to your board and get a follow-up reminder.
Draft a cover letter
An honest first draft from your resume and this job.
Prepare for interviews
Likely questions based on this job description.
About PSI CRO
Listing details & historyShowHide
- Employer posted
- 16 Oct 2026
- Last confirmed open
- 35 min ago
- Source
- Employer careers site
- Degree
- Degree preferred
- “Remote role in Ukraine Your responsibilities will include: Preparing, conducting, and reporting on all types of monitoring visits, including site selection, initiation, routine monitoring, and close-out visits Ensuring compliance with study protocols, ICH-GCP guidelines, and regulatory requirements Building and maintaining strong relationships with”
- Visa
- Not stated
- Timezone
- Not stated
- Languages
- English
- Location evidence
- “Remote (Kyiv, Kyiv city, Ukraine)”
Details are read from the listing text. They are not a guarantee of work authorization; confirm with the employer.