Clinical Research Associate - West Coast
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. Our client is looking for candidates with experience monitoring Ophthalmology trials or multi-TA.
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Willingness to travel as required (approximately 60%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
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
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
Responsibilities
Monitor clinical trials and coordinate study monitoring activities
Prepare and maintain study status reports and documentation
Ensure patient safety and regulatory compliance
Qualifications
University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines
English communication skills
Required Skills
clinical trial monitoringICH-GCPregulated drug developmentinvestigator liaisonsite management