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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
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
local regulatory requirements
maintain project timelines
Nice-to-have
effective communication
organizational skills
interpersonal skills
ability to work independently
prioritize tasks effectively
Key Requirements
Bachelor’s Degree in life sciences or related field
5 years’ clinical research experience
Knowledge of applicable regulatory requirements
Understanding of regulated clinical trial environment