Responsibilities:

• Pre-study visits, initiation visits, routine Monitoring visits, Сlose-Out visits;
• Assistance in training of Junior CRAs;
• Negotiations of clinical trials agreements with investigator sites and study budgets;
• Obtaining and reviewing of required study documents from investigator sites.

Requirements:

• English - Intermediate;
• Independent monitoring experience in clinical trials is a must;
• Ability to travel at least 65% of the working time.

Conditions:

• Salary is to be determined based on results of the interview.