Title: CRA II / Sr. CRA
Location: UAE
Job Purpose/Summary
As a CRA you will be responsible for the successful conduct of clinical trials and serve as main contact for the investigative site by representing Clinart in a professional manner.
What You’ll Do
- Serve as main Clinart contact for assigned study sites
- Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP
- Assist with or oversee study start-up activities, including feasibility, pre-study activities and site selection
- Collect, review and track essential/regulatory documents
- Participate in and complete all general and study specific training as required
- Participate in investigator, client and project team
