Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.
Requirements
Bachelor’s Degree in life sciences or a related field
3 years clinical research experience
1 year experience in a leadership capacity
In-depth knowledge of clinical systems, procedures, and corporate standards
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
