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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_4a60c2d2-e95"},"title":"Sr CRA - Southern California","description":"<p>As a Senior CRA at ICON Strategic Solutions, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p>You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:</p>\n<ul>\n<li>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p>You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li>\n<li>Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.</li>\n<li>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li>\n<li>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li>\n<li>Willingness to travel as required (approximately 60%)</li>\n<li>Candidates must be located in Southern California</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Los-Angeles-CA/Senior-CRA_JR161410","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON Strategic Solutions","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Los-Angeles-CA/Senior-CRA_JR161410","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$110,520.00-$138,150.00","x-skills-required":["Good Clinical Practice (GCP)","clinical trial monitoring","data integrity","site management","clinical trial software"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"required","x-work-authorisation-text":"Employment with ICON is contingent upon having the legal right to work in the country where the role is based.","datePosted":"2026-10-26T18:18:44.986Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Southern California"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical trial monitoring, data integrity, site management, clinical trial software","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":110520,"maxValue":138150,"unitText":"YEAR"}}}]}