Descrizione:
Experteer Overview
In this role you drive the operational management of assigned clinical projects, ensuring alignment with Chiesi’s goals and medical standards. You will coordinate with CROs, internal partners, and vendors to deliver studies on time and within budget. You’ll act as the primary operational contact for clinical trials and contribute to study design and risk management. This is an opportunity to shape multi-site trials in a global R&D environment and impact patient outcomes through rigorous study execution.
Retribuzione / Benefits
- Coordinate day-to-day operational management of 1–3 clinical trials, ensuring timelines and budgets are respected
- Act as primary operational contact for CROs and internal stakeholders; represent the Study Team for trial activities
- Review study documents from CROs (plans, risk, site contracts) and perform co-monitoring as needed
- Maintain Study Risk Register and drive follow-up actions with vendors
- Manage study eTMF with CTA and ensure compliance with SOPs and quality standards
- Prepare and coordinate scientific meetings and expert/KOL contracts as required
- Prepare/review CSR and support presentation of results; liaise with CTS on CTS strategy and execution
- Ensure budget planning and management for ongoing studies
Responsabilità
- At least 3 years of experience in a similar pharmaceutical role
- Track record of planning and executing 5+ clinical studies
- Degree in Life Sciences or equivalent
- English fluent
- Knowledge of clinical study design, Clinical Research Statistics, planning tools, ICH/GCP and SOPs
- GLP knowledge for bio-analytical assays (clinical pharmacology) and literature awareness
Requisiti fondamentali
- Hybrid and remote working options
- Pension
- Private medical insurance
- Wellbeing programme
- Flexible benefits programme
- Ticket restaurant
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