Senior Clinical Research Associate
Job Description
As a Senior 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, SSV, 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
- 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 participate on audits and inspections
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent
- site monitoring experience - Experience in all types of monitoring visits in Phase II and/or III studies
- Experience in Oncology, Infectious Diseases and IBD is a plus
- Full working proficiency in Romanian and English
- Proficiency in MS Office applications
- Valid driver’s license & ability to travel
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
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