Experienced Clinical Research Associate, Iqvia Biotech - Home Based, Italy
IQVIA seeks an experienced Clinical Research Associate to conduct site monitoring, manage study protocols, and ensure regulatory compliance across assigned clinical trials. The role involves site visits, recruitment coordination, data management, and documentation in accordance with GCP and ICH guidelines.
Responsibilities
Conduct site monitoring visits including selection, initiation, monitoring, and close-out activities per protocol and regulations
Work with sites to develop, track, and optimize subject recruitment plans aligned with study timelines
Administer protocol training to sites and maintain ongoing communication regarding expectations and issues
Evaluate site compliance with protocol requirements and applicable regulations; escalate quality concerns as needed
Track study progress including regulatory submissions, enrollment metrics, CRF completion, and data query resolution
Requirements
Bachelor's degree and Master's degree in scientific or healthcare discipline
CRA Certification per Italian Ministerial Decree dated **********
Experience in pharmaceutical industry or clinical trials environment
Advanced proficiency with MS Office and computer systems
Fluent English language skills, written and verbal
Strong organizational and problem-solving abilities
Valid Class B driver's license; willingness to travel
Compensation:
€34,300–€63,100 base annually
Responsibilities
Conduct site monitoring visits including selection, initiation, monitoring, and close-out activities per protocol and regulations
Work with sites to develop, track, and optimize subject recruitment plans aligned with study timelines
Administer protocol training to sites and maintain ongoing communication regarding expectations and issues
Evaluate site compliance with protocol requirements and applicable regulations; escalate quality concerns as needed
Track study progress including regulatory submissions, enrollment metrics, CRF completion, and data query resolution
Requirements
Bachelor's degree and Master's degree in scientific or healthcare discipline
CRA Certification per Italian Ministerial Decree dated **********
Experience in pharmaceutical industry or clinical trials environment
Advanced proficiency with MS Office and computer systems
Fluent English language skills, written and verbal
Strong organizational and problem-solving abilities
Valid Class B driver's license; willingness to travel
Compensation:
€34,300–€63,100 base annually