{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/mechelen/"},"x-facet":{"type":"city","slug":"mechelen","display":"Mechelen","count":2},"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_82d735f1-170"},"title":"Global Regulatory Lead","description":"<p>As a Global Regulatory Lead at ICON Strategic Solutions, you will provide strategic regulatory leadership across the development lifecycle of innovative therapeutics.</p>\n<p>You will work collaboratively with cross-functional stakeholders to drive patient-focused regulatory strategies, support accelerated development pathways, lead agency interactions, and ensure programs are positioned for successful transition into later-stage development.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Providing strategic global regulatory leadership for assigned early development programs</li>\n<li>Developing and executing innovative global regulatory strategies</li>\n<li>Embedding patient-focused approaches into regulatory planning and development strategies</li>\n<li>Serving as a key member of the Early Development Regulatory Team</li>\n<li>Representing Regulatory Affairs within governance committees and development forums</li>\n<li>Partnering closely with asset teams to facilitate seamless transition of programs</li>\n<li>Collaborating with regulatory leadership to establish and enhance processes</li>\n<li>Mentoring, coaching, and developing members of the regulatory organization</li>\n<li>Building and maintaining strong relationships with internal stakeholders</li>\n<li>Monitoring, assessing, and communicating evolving global regulatory requirements</li>\n<li>Leading interactions with health authorities and overseeing external regulatory vendors</li>\n<li>Providing hands-on support for key regulatory submissions and interactions</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in Life Sciences, Pharmacy, Medicine, or related scientific discipline</li>\n<li>At least 5-7 years of experience leading global regulatory strategies and teams</li>\n<li>Deep knowledge of global regulatory frameworks</li>\n<li>Demonstrated experience supporting innovative therapies through early clinical development</li>\n<li>Proven expertise in developing and implementing global regulatory strategies</li>\n<li>Experience conducting health authority interactions and submissions</li>\n<li>Strong leadership skills with the ability to influence without authority</li>\n<li>Excellent verbal, written, presentation, and stakeholder management skills</li>\n<li>Strong project management, prioritization, and organizational capabilities</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 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/Belgium-Mechelen/Early-Developement-Global-Regulatory-Lead_JR162620","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/Belgium-Mechelen/Early-Developement-Global-Regulatory-Lead_JR162620","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["global regulatory strategies","regulatory leadership","patient-focused approaches","health authority interactions","project management"],"x-skills-preferred":["advanced scientific degree","experience across both early and late-stage drug development","scientific expertise in Immunology","knowledge of diverse therapeutic modalities"],"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":"2026-10-27T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Mechelen"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"global regulatory strategies, regulatory leadership, patient-focused approaches, health authority interactions, project management, advanced scientific degree, experience across both early and late-stage drug development, scientific expertise in Immunology, knowledge of diverse therapeutic modalities"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_534a936f-243"},"title":"Snr CRA - Clinical Site Management","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 Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p><strong>Responsibilities</strong></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><strong>Your Profile</strong></p>\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</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\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/Belgium-Mechelen/Senior-Clinical-Research-Associate_JR159415","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/Belgium-Mechelen/Senior-Clinical-Research-Associate_JR159415","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","clinical trial monitoring","data integrity","site management","clinical trial software"],"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":"2026-10-29T21:29:38.563Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Mechelen"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical trial monitoring, data integrity, site management, clinical trial software"}]}