17 set - Muggiò
Iqvia
Overview
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In this role, you will support multinational clinical studies by coordinating site activities and ensuring high-quality data. You will work within a cross-functional team to monitor sites, manage regulatory submissions, and help optimize recruitment. You'll contribute to compliant trial conduct aligned with GCP and ICH standards, impacting patient outcomes and study success.
This is an international, growth-oriented opportunity with strong support for professional development and a stable, reputable employer.
Retribuzione / Benefits
- career growth resources
- flexible work schedules
- therapeutic knowledge programs
- company car
- mobile phone
- attractive benefits package
Responsabilità
- Perform site selection, initiation, monitoring and close-out visits
- Support development of a subject recruitment plan
- Evaluate quality and integrity of site practices per GCP/ICH
- Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions
- Collaborate with study site experts and client representatives
Requisiti fondamentali
- University Bachelor's Degree and Master's Degree in scientific discipline or health care
- CRA Certification as required by Ministerial Decree dated 15.11.2011
- Experience in Pharma Industry and/or Clinical Trials
- Very good computer xkiyazw skills including MS Office
- Excellent command of English
- Strong organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Flexibility to travel
- Driver's license class B
- communication
- collaboration
- problem-solving
- MS Office
- regulatory knowledge (GCP and ICH)
- clinical trial monitoring
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