Overview
In this field-based role, you will support European clinical trials by engaging investigators and site teams, offering scientific and protocol guidance, and driving patient enrolment. You will collaborate with study sites, sponsors, and cross-functional teams to strengthen recruitment strategies and ensure trial design and protocol requirements are clearly understood. You will build investigator relationships, provide training, and help translate best practices into practical actions, contributing to streamlined study delivery and enrolment outcomes across Europe.
Retribuzione / Benefits
- Competitive base salary
- Performance-related incentives
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
Responsabilità
- Build relationships with investigators, site staff and stakeholders to support trial delivery and recruitment.
- Provide scientific, clinical and protocol training to study teams to ensure understanding of study design and procedures.
- Develop and optimize site- and study-level enrolment strategies to improve recruitment and retention.
- Collaborate with cross-functional teams to translate best practices into local action.
- Represent the study at site visits, project meetings, and industry events.
- Support continuous improvement of enrolment processes and trial outcomes.
Requisiti fondamentali
- Doctoral degree (MD, PharmD or PhD)
- Experience in clinical research within Pharma, Biotech or CRO environments
- Strong scientific and medical knowledge with understanding of clinical development and local healthcare landscapes
- Established scientific and clinical network in Europe with networking, influencing and negotiation skills
- Excellent communication and presentation skills in English and Italian (additional EU languages advantageous)
- Ability to interpret complex medical data and apply technical, scientific and clinical knowledge
- Strong analytical, problem-solving and critical-thinking skills with attention to accuracy and compliance
- Proactive, self-motivated and able to work independently and collaboratively
- communication
- interpersonal skills
- networking
- clinical development knowledge
- data interpretation of complex medical information
- medical language proficiency in English and Italian
Clinical Trial Liaison in Pavia datore di lavoro: Icon Clinical PLC
Lavorare come Global Study Manager in questa azienda significa entrare a far parte di un ambiente stimolante e collaborativo, dove la tua esperienza nella gestione di studi clinici avrà un impatto diretto sullo sviluppo di nuovi farmaci. Offriamo un pacchetto retributivo competitivo, opportunità di crescita professionale e un forte impegno verso il benessere dei dipendenti, con benefit che includono copertura sanitaria, piani pensionistici e programmi di formazione continua. La nostra cultura aziendale è guidata da valori etici e dalla volontà di innovare, rendendo ogni giorno un'opportunità per contribuire a risultati significativi a livello globale.
