About the role

Clinical Research Associate monitoring sponsor-dedicated clinical trials at ICON, the global clinical research organization. Ensuring protocol compliance, data integrity, and patient safety across trial sites.

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 resolution of queries to maintain high-quality clinical data.
Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
Design and analyse clinical trials, interpret complex medical data, and contribute to innovative treatments and therapies.
Take responsibility for deliverables and work collaboratively in a sponsor-dedicated model.

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 as required (approximately 60%).
Legal right to work in the country where the role is based.

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