Note: The job is a remote job and is open to candidates in USA. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Responsibilities
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborating with investigators and site staff to facilitate smooth study conduct
- Performing data review and resolution of queries to maintain high-quality clinical data
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Skills
- Bachelor's degree in a scientific or healthcare-related field highly preferred
- 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
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license
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
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