{"data":{"company":{"name":"ICON plc","slug":"icon-plc","logo_url":"https://logos.yubhub.co/icon.com.png","canonical_domain":"icon.com","editorial":null,"wikidata_id":null,"founded":null,"ceo":null,"founders":[],"hq_location":null,"industry":null,"employee_count":null,"official_website":null,"wikipedia_url":null,"stock_ticker":null,"stock_price":null,"market_cap":null,"revenue":null,"ipo_date":null,"sector":null,"full_time_employees":null,"company_description":null,"twitter_username":null,"linkedin_id":null,"instagram_username":null,"facebook_id":null,"parent_org":null,"country":null,"github_org":null,"github_public_repos":null,"github_followers":null,"github_verified":0,"github_description":null,"github_location":null,"github_blog":null,"github_twitter":null,"stock_exchange":null,"stock_beta":null,"stock_range":null,"stock_is_actively_trading":null,"fmp_image":null,"fmp_address":null,"fmp_city":null,"fmp_state":null,"fmp_country":null,"recent_news":[],"search_interest_index":null,"search_interest_trend":null,"wikipedia_monthly_views":null,"hn_mention_count":null,"hn_top_stories":[],"wayback_first_year":null,"sec_incorporation_state":null,"sec_latest_filing_type":null,"sec_latest_filing_date":null,"sec_filings":[],"research_papers_count":null,"research_citations_count":null,"research_h_index":null,"research_topics":[],"is_federal_contractor":null,"earnings_calendar":[],"industry_canonical":null,"enrichment_sources":[],"last_enriched_at":null},"hiring":{"total_jobs":16,"categories":[{"category":"healthcare","count":14},{"category":"sales","count":2}],"experience_levels":[{"level":"senior","count":14},{"level":"mid","count":1}],"work_arrangements":[{"arrangement":"remote","count":9},{"arrangement":"onsite","count":2}],"top_titles":[{"title":"Senior CRA","count":4},{"title":"Account Development Manager","count":2},{"title":"Senior Medical Research Associate (Paramedic)","count":1},{"title":"Senior Clinical Trial Manager (US sites experienced) - Mexico / Brazil / Colombia / Peru / Chile - Remote","count":1},{"title":"Senior Clinical Trial Associate","count":1},{"title":"Senior Client Services Associate","count":1},{"title":"Project Manager FSA - EUROPE - Homebased","count":1},{"title":"Medical Technologists I, II and Senior","count":1},{"title":"Freelance Senior CRA","count":1},{"title":"CRA II - Greece - Remote","count":1},{"title":"Clinical Trial Manager, Japan","count":1},{"title":"(Senior) Clinical Trial Manager","count":1}],"locations":[{"location":"warsaw","count":3},{"location":"taipei","count":1},{"location":"lenexa, ks","count":1},{"location":"frankfurt","count":1},{"location":"farmingdale, ny","count":1},{"location":"buenos aires","count":1},{"location":"boston, ma","count":1},{"location":"blue bell (icon","count":1},{"location":"athens","count":1}],"skills":[{"skill":"Ich-gcp","required":3,"preferred":0,"total":3},{"skill":"Regulatory Requirements","required":3,"preferred":0,"total":3},{"skill":"Clinical Research","required":2,"preferred":1,"total":3},{"skill":"Monitoring Experience","required":0,"preferred":3,"total":3},{"skill":"Clinical Trial Monitoring","required":3,"preferred":0,"total":3},{"skill":"Good Clinical Practice GCP","required":3,"preferred":0,"total":3},{"skill":"Data Integrity","required":3,"preferred":0,"total":3},{"skill":"Site Management","required":3,"preferred":0,"total":3},{"skill":"CRM Management","required":2,"preferred":0,"total":2},{"skill":"Communication Skills","required":2,"preferred":0,"total":2},{"skill":"CRO Experience","required":0,"preferred":2,"total":2},{"skill":"English","required":2,"preferred":0,"total":2},{"skill":"Communication","required":2,"preferred":0,"total":2},{"skill":"Clinical Trial Management","required":2,"preferred":0,"total":2},{"skill":"Medicine","required":2,"preferred":0,"total":2},{"skill":"Science","required":2,"preferred":0,"total":2},{"skill":"Clinical Trials","required":2,"preferred":0,"total":2},{"skill":"Regulatory Guidelines","required":2,"preferred":0,"total":2},{"skill":"Therapeutic Area Expertise","required":0,"preferred":2,"total":2},{"skill":"Life Sciences","required":1,"preferred":0,"total":1}],"salary_stats":null,"job_types":[{"type":"full-time","count":10},{"type":"part-time","count":1},{"type":"contract","count":1}],"latest_jobs":[{"id":"job_4001ff17-123","title":"Senior CRA","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Poland-Warsaw/Senior-CRA_JR155645","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>ICON is seeking a Senior CRA to oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p>As a Senior CRA at ICON Plc, you will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.</p>\n<p>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</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>","enriched_at":1793312342312},{"id":"job_cbf2efc0-b57","title":"Senior Clinical Trial Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Poland-Warsaw/CRL-Assistant_JR158098","location":"Warsaw","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","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 Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges. Key responsibilities include:</p>\n<ul>\n<li>Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.</li>\n<li>Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.</li>\n<li>Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.</li>\n<li>Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.</li>\n<li>Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have a strong foundation in clinical trial management, 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 in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.</li>\n<li>Strong organisational and multitasking skills, with the ability to manage multiple tasks and projects effectively.</li>\n<li>Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.</li>\n<li>Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.</li>\n<li>Willingness to travel as required (approximately 10%)</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>","enriched_at":1793310710557},{"id":"job_a24cc61a-fbc","title":"Senior Client Services Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Senior-Client-Services-Associate_JR152226","location":null,"job_type":null,"experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>We are seeking a Senior Client Services Associate to support efforts to maintain and expand upon COA copyright holders and client relationships.</p>\n<p>The successful candidate will manage and grow existing copyright holder accounts, ensuring high levels of engagement and satisfaction.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Managing and growing existing copyright holder accounts</li>\n<li>Enhancing copyright holder satisfaction through proactive communication and value-added support</li>\n<li>Leading project management, monitoring, and reporting activities related to assigned accounts</li>\n<li>Building and expanding relationships with Clinical Outcome Assessment (COA) copyright holders and developers</li>\n<li>Coordinating the setup and implementation of distribution processes for new COAs</li>\n<li>Conducting due diligence activities to verify and document copyright ownership</li>\n<li>Serving as a subject matter expert in COA management</li>\n<li>Acting as the primary point of contact for assigned accounts</li>\n<li>Collaborating cross-functionally with licensing, legal, operations, and commercial teams</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>At least 2 years of client management experience</li>\n<li>Contract management experience</li>\n<li>Strong organisational and analytical skills</li>\n<li>Public speaking skills</li>\n<li>Advanced level of English</li>\n<li>Proficiency in Microsoft Office Suite (Word, Excel, PPT)</li>\n<li>Experience in clinical research field/COA field/pharma industry/Project Management is a plus</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>","enriched_at":1793306467621},{"id":"job_bec34cc3-ac4","title":"Account Development Manager","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Account-Development-Manager_JR162284","location":"Boston, MA","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Sales","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 values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>This is a fully remote opportunity; however, preference will be given to candidates located in the Greater Boston, MA area due to the strategic importance of the Boston biotechnology and pharmaceutical market and opportunities for local client engagement, networking, and industry event participation.</p>\n<p><strong>About the job</strong></p>\n<p>ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.</p>\n<p><strong>Who are you?</strong></p>\n<ul>\n<li>You are someone with a deep burning desire to succeed despite obstacles that may present themselves</li>\n<li>A strategic thinker, you will continue to develop new ways to contact key decision makers at biotech, pharmaceutical and medical device/diagnostic companies, both large and small</li>\n<li>You are an expert at building and cultivating relationships. Persistent and tenacious, you are also keenly aware of when to pull back and wait patiently for the right time</li>\n<li>You are a hunter, always looking for new clients and most importantly, you are a team player who will add a sense of humor, experience, and enthusiasm to our Account Development team</li>\n</ul>\n<p><strong>Primary Responsibilities</strong></p>\n<ul>\n<li>Increase market awareness, sales and profitability by increasing the number of new Requests for Proposals (RFPs)</li>\n<li>Work closely with Account Executives and engagement partners to create a plan to enhance new account penetration, meetings, and RFPs</li>\n<li>Call new and existing accounts and schedule meetings for the business development team</li>\n<li>Regularly follow-up with prospective clients to build meaningful relationships</li>\n<li>Maintain and manage CRM with all activity</li>\n<li>Generate reports to highlight RFPs, meetings, and new account penetration</li>\n<li>Research accounts and identify new opportunities for ICON</li>\n<li>Provide updates to the business development team on activity and conversations with clients</li>\n<li>Generate client interest for potential webinars, industry meetings and conferences</li>\n<li>Review metrics on a regular basis to assess productivity</li>\n<li>Attend internal meetings to discuss new opportunities and the sales pipeline</li>\n<li>Support the preparation for client meetings</li>\n<li>Develop a sales methodology and strategy for increasing new account penetration</li>\n<li>Learn messaging around ICON’s differentiators</li>\n<li>Lead calls and participate in client meetings</li>\n<li>Execute against a specific account plan; routinely achieving quarterly objectives</li>\n</ul>\n<p><strong>To be Successful in the Role, you will have:</strong></p>\n<ul>\n<li>Undergraduate degree or its international equivalent from an accredited institution or equivalent experience</li>\n<li>Pre / inside sales experience or related experience that requires communicating with potential clients</li>\n<li>Strong verbal and written communication skills</li>\n<li>Familiarity with maintaining and managing a customer relationship database</li>\n<li>Preferably 1-2 years of CRO experience</li>\n<li>Knowledge of the Greater Boston life sciences market, including key biotechnology, pharmaceutical, and healthcare stakeholders, strongly preferred.</li>\n<li>Candidates located in the Boston metropolitan area are strongly preferred, though remote candidates within the United States will be considered.</li>\n</ul>\n<p><strong>What ICON can offer you:</strong> 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 and OTE, 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.</p>\n<p><strong>Rewards &amp; Benefits</strong> 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>","enriched_at":1793228502705},{"id":"job_4bf94e77-cd6","title":"Project Manager FSA - EUROPE - Homebased","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Poland-Warsaw/Project-Manager--Feasibility-Site-Activation_JR159283","location":"Warsaw","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","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 Project Manager – Feasibility &amp; Site Activation, you will play a critical role in driving the successful start-up of global clinical studies.</p>\n<p>This is a highly visible position where you will take ownership of the Study Start-Up (SSU) strategy and execution,ensuring that sites are activated efficiently, regulatory pathways are navigated effectively, and studies are positioned for successful delivery from day one.</p>\n<p>You will work at the center of cross-functional collaboration, partnering with sponsors, internal teams, and sites worldwide to deliver start-up excellence at scale.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Shape and execute Study Start-Up strategies across global, multi-country studies, ensuring alignment with timelines, scope, and sponsor expectations</li>\n<li>Lead the development and delivery of comprehensive Study Start-Up Plans, covering regulatory, ethics, and contract execution across all participating countries</li>\n<li>Drive end-to-end start-up activities from site identification through to IP release, maintaining momentum and accountability for key milestones</li>\n<li>Provide strategic input at Bid Defence and Kick-Off meetings, influencing study design and start-up feasibility from the outset</li>\n<li>Oversee regulatory and ethics submissions, ensuring high-quality, compliant, and timely approvals across regions</li>\n<li>Manage site contract and budget negotiations in collaboration with legal, finance, and sponsors, supporting timely site activation</li>\n<li>Proactively identify risks, dependencies, and bottlenecks, implementing mitigation and escalation strategies to protect study timelines</li>\n<li>Partner closely with Project Managers and cross-functional stakeholders, ensuring seamless integration of start-up within overall study delivery</li>\n<li>Ensure accuracy, quality, and inspection readiness of all study documentation, including oversight of CTMS and eTMF activities</li>\n<li>Lead and coordinate Study Start-Up team members, providing direction, support, and oversight to ensure consistent delivery</li>\n<li>Drive process consistency and continuous improvement across regions, contributing to operational excellence initiatives</li>\n<li>Maintain oversight of study metrics, budgets, and scope of work (SOW), ensuring delivery within agreed parameters</li>\n<li>Provide clear, structured reporting and updates to sponsors and internal leadership, enabling informed decision-making</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in Life Sciences or a related field</li>\n<li>Recent Study Start-Up (SSU) experience with end-to-end site activation responsibility</li>\n<li>Experience supporting global and multi-country clinical trials</li>\n<li>Strong knowledge of CA/EC submissions, CTA processes, and regulatory requirements</li>\n<li>Experience managing site contracts, budgets, and start-up timelines</li>\n<li>Working knowledge of CTMS, eTMF, and other clinical systems</li>\n<li>Solid understanding of ICH-GCP and applicable regulations</li>\n<li>Strong stakeholder management, communication, and collaboration skills</li>\n<li>Organized, proactive, and solution-oriented approach</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>","enriched_at":1793209428639},{"id":"job_f19c3f03-450","title":"Senior Clinical Trial Manager (US sites experienced) - Mexico / Brazil / Colombia / Peru / Chile - Remote","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Senior-Clinical-Trial-Manager_JR161323","location":null,"job_type":null,"experience_level":"senior","work_arrangement":"remote","category":"Healthcare","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. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.</p>\n<p><strong>Responsibilities</strong></p>\n<p>Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. Key responsibilities include:</p>\n<ul>\n<li>Budget Oversight: Oversee the clinical portion of the budget to ensure efficient resource allocation.</li>\n<li>Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.</li>\n<li>Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.</li>\n<li>Timely Study Start-Up &amp; Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.</li>\n<li>Improving Study Integrity: Review trip reports and implement corrective and preventative action plans when necessary.</li>\n<li>Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<p>You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:</p>\n<ul>\n<li>A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.</li>\n<li>Bachelor&#39;s degree in health, life sciences, or other relevant fields of study.</li>\n<li>At least 10+ years of relevant experience in clinical trial management.</li>\n<li>Preferred: 2+ years of monitoring experience.</li>\n<li>Experience supporting complex protocols, including areas such as MASH/NASH, Radiopharmaceutical, or other specialized therapeutic programs, is highly valued.</li>\n<li>Experience in managing complex or global trials is advantageous.</li>\n<li>Preferred: Experience in managing all trial components from start-up to database lock.</li>\n<li>This role is intended for experienced CTM professionals; entry-level CTM experience alone will not meet the requirements.</li>\n<li>Willingness to travel as required (approximately 25%).</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>Benefits may vary depending on role and location.</p>","enriched_at":1793190687857},{"id":"job_f3a80f14-7c1","title":"(Senior) Clinical Trial Manager","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Taiwan-Taipei/XMLNAME--Senior--Clinical-Trial-Manager_JR159299","location":"Taipei","job_type":null,"experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>ICON is seeking a Senior Clinical Trial Manager to oversee the planning, execution, and completion of clinical trials. You will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive successful trial outcomes.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.</li>\n<li>Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.</li>\n<li>Build and manage strong relationships with trial investigators and stakeholders.</li>\n<li>Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.</li>\n<li>Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>University degree in medicine, science, or equivalent combination of education &amp; experience</li>\n<li>Demonstrated ability to drive the clinical deliverables of a study</li>\n<li>Subject matter expertise in the designated therapeutic area</li>\n<li>Prior monitoring experience is preferred</li>\n<li>Ability to travel up to 20%</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>","enriched_at":1793186635073},{"id":"job_845d26c1-ce0","title":"Clinical Trial Manager, Japan","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Japan-Tokyo/Clinical-Trial-Manager_JR148241","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>ICON is seeking a Clinical Trial Manager to oversee the planning, execution, and completion of clinical trials in Japan.</p>\n<p>As a Clinical Trial Manager, you will be responsible for managing all aspects of clinical trials, collaborating with cross-functional teams, building relationships with trial investigators and stakeholders, and ensuring compliance with regulations and guidelines.</p>\n<p>Key responsibilities:</p>\n<ul>\n<li>Plan and manage clinical trials, ensuring adherence to timelines, budgets, and quality standards</li>\n<li>Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures</li>\n<li>Build and manage strong relationships with trial investigators and stakeholders</li>\n<li>Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines</li>\n<li>Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>University degree in medicine, science, or equivalent combination of education and experience</li>\n<li>Demonstrated ability to drive clinical deliverables of a study</li>\n<li>Subject matter expertise in the designated therapeutic area</li>\n<li>Prior monitoring experience is preferred</li>\n<li>Ability to travel up to 20%</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package, including:</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</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>","enriched_at":1793168778662},{"id":"job_1af79d55-ca8","title":"CRA II - Greece - Remote","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Greece-Athens/CRA-II_JR144752","location":"Athens","job_type":"full-time","experience_level":"mid","work_arrangement":"remote","category":"Healthcare","description":"<p>ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.</p>\n<p>We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.</p>\n<p><strong>What you will be doing</strong></p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your profile</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 2 years of experience as a Clinical Research Associate.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Strong organizational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver&#39;s license.</li>\n</ul>\n<p><strong>What ICON can offer you:</strong></p>\n<p>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.</p>\n<p>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.</p>\n<p>Our benefits examples include:</p>\n<ul>\n<li>Various annual leave entitlements.</li>\n<li>A range of health insurance offerings to suit you and your family’s needs.</li>\n<li>Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</li>\n<li>Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.</li>\n<li>Life assurance.</li>\n<li>Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</li>\n</ul>","enriched_at":1793168063857},{"id":"job_f2d57b30-ef7","title":"Senior CRA","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Argentina-Buenos-Aires/Senior-Clinical-Research-Associate_JR159324","location":"Buenos Aires","job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","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>Open to work with vaccine protocols.</li>\n<li>Willingness to travel as required (approximately 30%)</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>","enriched_at":1793136246309}],"category_normalised":[{"category":"healthcare","count":14},{"category":"sales","count":2}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":3},{"week_start":"2026-10-26","count":13}],"trend":"stable","wow_pct":333},"momentum":{"recent_14d":16,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":null,"industry_median":null,"percentile":null,"sample_size":0,"by_region":[],"transparency_pct":6,"industry_transparency_pct":0,"transparency_warning":true},"market_share":{"company_jobs":16,"industry_total":16,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.085,"skill_weighted_score":0.061,"top_exposed_titles":[{"title":"Account Development Manager","count":2,"score":0.069}],"top_exposed_skills":[{"skill":"Monitoring Experience","count":3,"score":0.061}]},"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"EU","count":4,"share_pct":36.4},{"region":"United States","count":3,"share_pct":27.3},{"region":"Unknown","count":2,"share_pct":18.2},{"region":"Latin America","count":1,"share_pct":9.1},{"region":"APAC","count":1,"share_pct":9.1}],"emerging":[{"region":"EU","recent_30d":4,"prior_30d":0,"growth_pct":100},{"region":"United States","recent_30d":3,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":0,"exec_prior_90d_avg":0,"exec_growth_pct":0,"notable_exec_hires":[]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":6}}}}