As a Clinical Research Associate II 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 inhouse 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 participate on audits and inspections
Qualifications :
- College/University degree in Life Sciences or an equivalent combination of education training & experience
- At least 2 years of independent onsite 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 problemsolving skills
- Ability to travel
- Valid drivers license
Additional Information :
What We Offer:
- Stability longterm cooperation
- Permanent contract fulltime 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 onthe 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.
Remote Work :
Yes
Employment Type :
Fulltime