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
Job Summary
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.
Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Matching Summary
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.
Skills & Requirements
Must-have
Site Activation activities
country level tasks
investigative sites SPOC
regulatory documents review
clinical systems knowledge
GCP/ICH guidelines
Nice-to-have
negotiating and communication skills
effective organizational skills
ability to work independently
manage multiple projects
Key Requirements
3 years clinical research experience
1 year leadership capacity experience
Bachelor’s Degree in life sciences
Knowledge of applicable regulatory requirements
Understanding of regulated clinical trial environment