About the job

The company is the largest regional CRO in Central and Eastern Europe with 10 offices in the region.

Due to the expansion of our operations in Croatia we are looking for CRA colleagues with at least 2 years of active monitoring experience. The package includes competitive salary, various performance bonus options and benefits.

Regular training programs are maintained for our CRAs. We take special attention to the balance of the work and your private life.

Main duties and responsibilities

• Initiate, monitor and close-out clinical studies
• Prepare and perform regulatory and ethics submission (drug, medical device, non-interventional)
• Support contracting procedure between Sponsor and Investigational sites;
• Perform feasibilities and pre-study evaluations;
• Document activity in accordance with ICH-GCP and standard operation procedures of the company;
• Prepare a summary (report) of activities as requested by the Manager.

Requirements:

• Bachelor degree in life sciences
• At least 2 years experience in CRA role
• Advanced level of English
• Confident IT skills
• Driver’s license
• Effective communication, customer focus, teamwork, time management, motivation to learn and develop

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