Clinical Research Associate
Overview
In this CRA II role, you monitor and support clinical trials within ICON’s sponsor-dedicated model, applying global expertise to ensure data quality and patient safety. You work with investigators and site staff to drive compliant study conduct and timely documentation. The position blends independent work with cross-functional collaboration in a fast-paced environment. You’ll contribute to trials that advance new treatments for patients and vantaggi from a structured development path.
Retribuzione / Benefits
- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities
Responsabilità
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout the trial
- Collaborate with investigators and site staff to facilitate 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 CSRs
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
- attention to detail
- self-motivation and independence
- clinical trial processes
- ICH-GCP guidelines
- data review and query resolution
In this CRA II role, you monitor and support clinical trials within ICON’s sponsor-dedicated model, applying global expertise to ensure data quality and patient safety. You work with investigators and site staff to drive compliant study conduct and timely documentation. The position blends independent work with cross-functional collaboration in a fast-paced environment. You’ll contribute to trials that advance new treatments for patients and vantaggi from a structured development path.
Retribuzione / Benefits
- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities
Responsabilità
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout the trial
- Collaborate with investigators and site staff to facilitate 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 CSRs
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
- attention to detail
- self-motivation and independence
- clinical trial processes
- ICH-GCP guidelines
- data review and query resolution