Description
As a Clinical Research Associate (CRA II) at ICON Strategic Solutions, you will work in a sponsor-dedicated model supported by ICON's global expertise.
You will design and analyse clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies. Your client is looking for candidates with experience monitoring Ophthalmology trials or multi-therapeutic areas.
Responsibilities:
- 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 resolve queries to maintain high-quality clinical data.
- Contribute to preparing and reviewing study documentation, including protocols and clinical study reports.
Your Profile:
- 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 organisational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%).
Rewards & 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.
Inclusion and Accessibility:
ICON is an equal opportunity employer committed to building an inclusive and accessible workplace where everyone feels valued and supported.