28 ott - Monza
Psi Cro
Overview
Di seguito troverà tutto ciò che deve sapere su questa occasione e sui requisiti richiesti ai candidati.
In this role you will drive study startup activities to ensure timely activation of clinical sites in Italy. You will partner with project teams, sites, vendors, and review bodies to streamline ethics, regulatory submissions, and site activation. You’ll monitor startup timelines, optimize processes, and contribute to a global pharmacovigilance-minded mission. This position blends hands-on coordination with process improvement in a hybrid Milan setting, offering growth within a patient-focused pharmaceutical environment.
Retribuzione / Benefits
- base salary 31,700 – 40,150 gross annual salary
- bonus
- incentive plans
- other benefits may apply
- professional development opportunities
Responsabilità
- Support site identification and selection process
- Collect and review documents for ethics and regulatory review and approval
- Prepare site document packages for drug release to clinical sites
- Prepare and negotiate site contracts and budgets
- Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding startup matters until site activation
- Monitor startup metrics and timelines
- Coordinate initiatives for startup process improvement, analyze best practices and challenges
Requisiti fondamentali
- College/University degree or equivalent education/experience
- At xjncmbx least 1 year of industry experience in clinical research and/or at least 1 year of Study Startup experience in Italy
- Full working proficiency in English
- Strong communication and organizational skills
- Ability to negotiate and build relationships at all levels
- communication
- organizational skills
- negotiation
- ethics and regulatory submission
- site activation processes
- contract and budget negotiation
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