Clinical Research Associate - Remote
Overview In this role you will advance clinical studies by leading on-site and remote monitoring, ensuring data integrity and site partnership. You will drive study ownership across multiple sponsors and therapeutic areas, with a focus on deeper study knowledge and strong site relationships in Italy. You'll mentor less experienced CRAs and operate in a trusted, autonomous setup. This is an international, cross-functional environment with meaningful impact on clinical trial success.
Retribuzione / Benefits
base salary range 41.000–51.900 gross annual salary
premio
incentive plans
other benefits
Responsabilità
Conduct and report on-site monitoring visits and remote visits
Perform CRF review, source data verification and query resolution
Manage site communications and relationships
Participate in site identification
Assist in training less experienced CRAs
Lead assigned studies with ownership and cross-sponsor collaboration
Support deeper study focus with fewer protocols in Italy
Requisiti fondamentali
College/University degree in Life Sciences or equivalent
Independent on-site monitoring experience in Italy
Experience in Phase II and/or III monitoring visits
Full working proficiency in English
Proficiency in MS Office
Strong planning, multitasking and teamwork abilities
Excellent communication, collaboration and problem-solving skills
Ability to travel and hold a valid driver's license
communication
collaboration
problem-solving
MS Office applications
on-site monitoring
CRF review
Retribuzione / Benefits
base salary range 41.000–51.900 gross annual salary
premio
incentive plans
other benefits
Responsabilità
Conduct and report on-site monitoring visits and remote visits
Perform CRF review, source data verification and query resolution
Manage site communications and relationships
Participate in site identification
Assist in training less experienced CRAs
Lead assigned studies with ownership and cross-sponsor collaboration
Support deeper study focus with fewer protocols in Italy
Requisiti fondamentali
College/University degree in Life Sciences or equivalent
Independent on-site monitoring experience in Italy
Experience in Phase II and/or III monitoring visits
Full working proficiency in English
Proficiency in MS Office
Strong planning, multitasking and teamwork abilities
Excellent communication, collaboration and problem-solving skills
Ability to travel and hold a valid driver's license
communication
collaboration
problem-solving
MS Office applications
on-site monitoring
CRF review