Clinical Research Associate II
2 giorni fa
Varese, Lombardia, Italia
PSI CRO
Tempo pieno
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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
* bonus
* 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
* base salary range 41.000–51.900 gross annual salary
* bonus
* 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