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.
Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
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
Contract negotiations with research sites
Adherence to SOPs and Work Instructions
Quality control of documents
Maintain internal systems and databases
Nice-to-have
Local expertise for timeline planning
Direct contact with sponsors
Excellent prioritization skills
Excellent communication skills
Key Requirements
+2 years clinical research experience
Health Sciences degree
Advanced command of English language
GCP/ICH and applicable regulatory guidelines knowledge