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 SIV, RMV, COV onsite monitoring visits
- 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
- Prepare and particiapte on audits and inspections
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- At least 2 years of independent on-site monitoring experience in Hungary
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and Hungarian
- 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
- Valid driver’s license
What We Offer:
- Stability, long-term cooperation
- Permanent contract, full-time job
- Hybrid work setting (home and office based)
- Competitive salary and benefit package
- Company car, laptop and mobile phone
- Career development
- Unique combination of team collaboration and independent work
- Friendly and supportive colleagues
- Onboarding courses about clinical research industry
- Mentoring and on-the job training
- Comfortable and well established office
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
