Clinical Research Associate II
1 day ago
We are seeking a highly motivated Clinical Research Associate II to join our team as a Study Site Coordinator. In this role, you will be responsible for conducting and reporting onsite monitoring visits, driving study startup phases, and performing CRF reviews.
About UsPsi CRO Ag is a leading Contract Research Organisation with nearly 30 years of experience in delivering quality and on-time services across various therapeutic indications. We focus on building strong relationships with clinical sites and investigators, ensuring timelines, targets, and standards of clinical research projects.
Key Responsibilities- Conducting onsite monitoring visits, including interviews with site staff and review of source documents
- Driving the study startup phase, including setting up and managing site communication
- Performing CRF reviews and source document verification
- Supervising study activities, timelines, and schedules for each site
- Acting as a point of contact for in-house support services and vendors
- Degree in Life Sciences or equivalent combination of education, training & experience
- At least 2-3 years of experience conducting independent onsite monitoring visits, ideally on multiple projects at a time
- Demonstrable experience in all types of monitoring visits in Phase II and/or III
- Full and clean driver's license and ability to travel
- Excellent communication, collaboration, and problem-solving skills
We offer a competitive salary of approximately €55,000 - €65,000 per annum, depending on experience. Additionally, we provide opportunities for professional development and growth within the company.
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