As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
ResponsibilitiesWhat will you be doing?
Works on multiple trials within Oncology - Start up focus Collaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements.Perform Site Qualification Visits (SQVs) to assess the eligibility of sites for participation in specific clinical studies.Build strong relationships with site personnel to facilitate a smooth onboarding process.Ensure that all activities adhere to ICH-GCP guidelines, local regulatory standards, and internal Standard Operating Procedures (SOPs).Coordinate with the country operations team to collect essential documents (such as regulatory approvals and contracts) to enable timely site activation.Act as the main point of contact for sites, study teams, and external stakeholders throughout the start-up process.Work closely with the country operations team to manage investigator contracts, regulatory documents, and site-specific start-up activities.Provide regular status updates to both internal and external stakeholders, ensuring alignment with important project milestones.Monitor, report on, and analyze key performance indicators (KPIs) related to site selection and start-up timelines.Proactively identify and address any issues that may delay study initiation or affect trial deliverables.Maintain precise documentation to ensure readiness for inspections.Support sites during the activation phase until they achieve “Green Light” status for site opening.Facilitate coordination with site staff to ensure all pre-study requirements, including contracts, budgets, and essential documentation, are met.Possibly assist in audit and inspection preparations to guarantee compliance with regulatory and ethical standards.
Qualifications
What do you need to have?
Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological SciencesMust be located in California near a major airport Have a minimum of 2-3 years’ experience in monitoring pharmaceutical industry clinical trialsHave a minimum of 1-3 years' experience monitoring Oncology trials Knowledge of several therapeutic areasAnalytical/risk-based monitoring experience is an assetAbility to actively drive patient recruitment strategies at assigned sitesAbility to partner closely with investigator and site staff to meet all of our study timelinesAbility to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards/metrics, IWRS, safety reporting).Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently.Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.Pay Range ($89,376.00 USD – $111,720.00 USD)
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.