13 ott - Milano
Psi Cro
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
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