Overview
In this role, you contribute to the design, analysis, and oversight of clinical trials to support faster access to innovative therapies. You will perform monitoring activities, ensure patient safety, data integrity, and protocol compliance within a collaborative team. You’ll work with investigators and site staff to keep studies on track and deliver high-quality study documentation. This position offers the chance to impact patient care at a global, value-driven organization with opportunities for professional growth.
Retribuzione / Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Responsabilità
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation, including protocols and clinical study reports
Requisiti fondamentali
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Willingness to travel approximately 60%
- Strong communication skills
- Attention to detail
- Ability to work both independently and in a team
- Collaborative mindset in fast-paced environments
- ICH-GCP guidelines
- Clinical trial processes knowledge
CRA II 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.
