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.
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.
Develops professional individual contributor who works under moderate oversight and supervision, responsible for making recommendations for enhancements in systems and processes.
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
clinical research experience
GCP/ICH guidelines
regulatory requirements
project timelines adherence
document quality control
Nice-to-have
negotiating and communication skills
effective prioritization
problem-solving skills
team collaboration
Key Requirements
Bachelor’s Degree in life sciences or related field
5 years’ clinical research experience
Equivalent combination of education, training and experience