{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/lund/"},"x-facet":{"type":"city","slug":"lund","display":"Lund","count":1},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_14ab3b89-895"},"title":"Site Specialist II","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies.</li>\n<li>Acting as an operational liaison for site staff on documentation, systems, and process-related questions.</li>\n<li>Deliver regulatory submissions in accordance with contractual timelines, budget, and quality standards.</li>\n<li>Contribute to strategic planning of submissions to Regulatory Authorities (RA), Central Ethics Committees (CEC), and other applicable bodies.</li>\n<li>Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools.</li>\n<li>Supporting planning and logistics for site meetings, investigator meetings, and monitoring visits.</li>\n<li>Identifying opportunities to streamline site workflows and contributing to process improvement initiatives.</li>\n<li>Providing guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience.</li>\n<li>Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare.</li>\n<li>Experienced with a minimum of 3 years’ relevant regulatory experience in clinical research.</li>\n<li>Fluent in Swedish and English.</li>\n<li>Good understanding of clinical trial processes, GCP, and site documentation requirements.</li>\n<li>Strong organisational and problem-solving skills, with the ability to manage multiple sites and priorities.</li>\n<li>Excellent communication and interpersonal skills, with a proactive, service-focused mindset.</li>\n<li>Comfort working independently while collaborating effectively with cross-functional teams.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></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/Sweden-Lund/Site-Specialist-II_JR159903","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","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/Sweden-Lund/Site-Specialist-II_JR159903","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["life sciences","healthcare","business","clinical research","regulatory experience","GCP","site documentation","organisational skills","problem-solving skills","communication skills","interpersonal skills","Swedish","English"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental"],"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":"2026-10-26T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Lund, Sweden"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"life sciences, healthcare, business, clinical research, regulatory experience, GCP, site documentation, organisational skills, problem-solving skills, communication skills, interpersonal skills, Swedish, English"}]}