{"data":{"company":{"name":"ICON","slug":"icon","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":70,"categories":[{"category":"healthcare","count":55},{"category":"operations","count":2},{"category":"logistics 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Writing","required":4,"preferred":0,"total":4},{"skill":"Analytical Skills","required":4,"preferred":0,"total":4}],"salary_stats":null,"job_types":[{"type":"full-time","count":55},{"type":"prn/as needed","count":3},{"type":"contract","count":2}],"latest_jobs":[{"id":"job_fbcb36d1-c44","title":"Medical Monitor","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/United-States-of-America/Medical-Monitor_JR156527","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>ICON is seeking a Medical Monitor to provide medical leadership and strategic direction to clinical development programs.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Providing medical and scientific oversight for clinical trials, ensuring that study protocols are scientifically sound and aligned with regulatory requirements.</li>\n<li>Collaborating with clinical operations, regulatory, and safety teams to drive the successful execution of clinical development programs.</li>\n<li>Developing and reviewing clinical study protocols, investigator brochures, and other key study documents.</li>\n<li>Interpreting clinical trial data and providing medical insights to inform decision-making and guide clinical development strategies.</li>\n<li>Building relationships with key opinion leaders, investigators, and external stakeholders to support clinical development initiatives.</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Medical degree (MD) or equivalent qualification.</li>\n<li>Extensive experience in clinical research and development, preferably within the pharmaceutical or biotechnology industry.</li>\n<li>Strong understanding of clinical trial design, regulatory requirements, and GCP guidelines.</li>\n<li>Exceptional analytical and problem-solving skills, with a focus on interpreting clinical data and driving evidence-based decisions.</li>\n<li>Excellent leadership, communication, and collaboration skills, with the ability to work effectively in cross-functional, global teams.</li>\n<li>Willingness to travel as required (approximately 10%).</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":1793010851878},{"id":"job_8fc404ea-bd4","title":"Contract Analyst I","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Contract-Analyst-I_JR156987","location":null,"job_type":"contract","experience_level":"entry","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. As a Contract Analyst I at ICON, you will prepare, verify, and carry out invoicing via electronic processing and reporting activities for an assigned portfolio of accounts.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Negotiate directly with assigned sites on all site-related contracting items, including clinical trial agreements, budgets, payment terms, ancillary agreements, and amendments.</li>\n<li>Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&amp;C metrics and deliver processes.</li>\n<li>Ensure standards are applied to the SB&amp;C processes across projects.</li>\n<li>Leverage leading industry tools and data sources to provide budget and contract feedback aligned with parameters and fair market value guidance.</li>\n<li>Promptly recognise and improve potential delays and escalate to appropriate team members.</li>\n<li>Track all actions and negotiations to ensure timelines are achieved for studies and sites assigned.</li>\n<li>Support resolving escalated issues identified by the site activation sub-team in partnership with the internal Study Startup team.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>BS degree or international equivalent.</li>\n<li>2 or more years of experience in clinical research site contracting and budgeting within a pharmaceutical company, CRO, or relevant industry vendor.</li>\n<li>Ability to explain data to facilitate decision-making processes to be data-driven.</li>\n<li>Knowledge and understanding of clinical study protocols and schedule of assessments.</li>\n<li>Strong organisational skills, decision-making, communication, and negotiation skills.</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":1793010851657},{"id":"job_56d15b9d-bb7","title":"Senior Clinical Research Coordinator (Oncology)","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Downers-Grove-IL/Clinical-Research-Coordinator-Level-1_JR156823","location":"Lisle, IL","job_type":"full-time","experience_level":"senior","work_arrangement":"onsite","category":"Healthcare","description":"<p>ICON is seeking a Senior Clinical Research Coordinator (Oncology) to join Accellacare, part of ICON&#39;s clinical research network.</p>\n<p>As a Senior CRC, you will be accountable for seeking and completing clinical trial assignments in an autonomous, accurate, and timely manner in accordance with the SOP’s, COG’s and ICH guidelines.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Performing study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening patients</li>\n<li>Anticipating and planning for the logistical needs and requirements for any clinical trial, and assisting CRC Level I and Level II with the planning and conduct of trials</li>\n<li>Anticipating the specific recruitment needs and constantly evaluating the recruitment needs for any clinical trial and communicating recruitment efforts to the Manager of Clinical Operations</li>\n<li>Developing and executing recruitment plans that generate randomized patients and maximizing patient retention rates</li>\n<li>Attending investigator meetings</li>\n<li>Completing training on Clinical Trial Management System and maintaining proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment</li>\n<li>Performing technical requirements of the study protocol and training others in regards to technical requirements of a protocol</li>\n<li>Performing continuous reviews of the inclusion and exclusion criteria for each patient during the screening period</li>\n<li>Documenting laboratory data and adverse reactions, presenting this information to an investigator in a timely manner, and immediately notifying investigators, the Institutional Review Board and sponsor of any serious adverse events</li>\n<li>Dispensing study medication at the direction of the Investigator</li>\n<li>Establishing relationships with patient volunteers, and participating in patient education regarding the clinical trial process and providing specific trial information to the participant as well as conducting the informed consent process</li>\n<li>Working with investigators by communicating the status of patients referred, overall recruitment status, and clinical needs of the study</li>\n<li>Maintaining communication with the monitor from the sponsoring company through telephone contact, written communication, and on-site visits</li>\n<li>Establishing strong relationships with monitors and sponsors</li>\n<li>Proactively promoting the site with monitors and in-house contacts for future trials</li>\n<li>Engaging in prospecting for new potential business with our current customers and new customers</li>\n<li>Developing new physician relationships, and enhancing or leveraging the involvement of our current physician investigators</li>\n<li>Internal monitoring and review of other coordinators and support staff</li>\n<li>Attending site evaluation visits as a senior staff representative</li>\n<li>Assisting in the training and development of support and other site personnel</li>\n<li>Travel to other Duly sites within the Accellacare Site Network</li>\n</ul>\n<p>Profile:</p>\n<ul>\n<li>Oncology Clinical Research industry experience</li>\n<li>3+ years of experience as a Clinical Research Coordinator</li>\n<li>Clinical skills, such as phlebotomy</li>\n<li>Good understanding of clinical trial processes, GCP, and site documentation requirements</li>\n<li>Excellent time management and planning skills with an organized approach to work</li>\n<li>Bachelor’s degree in life sciences, healthcare, or a related field</li>\n</ul>\n<p>Rewards &amp; Benefits:</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":1793010258379},{"id":"job_3832f998-3c6","title":"Clinical Trial Supply Manager","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Bulgaria-Sofia/Clinical-Trial-Supply-Manager_JR155200","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Logistics & Supply Chain","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 Clinical Trial Supply Manager at ICON, you will oversee project and programme management workstreams, ensuring deliverables meet quality and timeline expectations.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Overseeing the planning and execution of clinical supplies projects, ensuring timely delivery and compliance with regulatory requirements.</li>\n<li>Collaborating with cross-functional teams to design and implement effective strategies for clinical trial supply management.</li>\n<li>Monitoring and analysing project timelines, budgets, and resource allocations to optimise efficiency and meet project goals.</li>\n<li>Addressing potential risks and challenges in clinical supplies logistics, proposing and implementing solutions to ensure smooth project execution.</li>\n<li>Fostering strong relationships with internal and external stakeholders, facilitating effective communication and collaboration throughout the project lifecycle.</li>\n</ul>\n<p>You will have solid project and programme management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant field, such as pharmacy, life sciences, or supply chain management.</li>\n<li>Proven experience in clinical supplies project management within the pharmaceutical or biotech industry.</li>\n<li>Strong understanding of regulatory requirements related to clinical trial supply management.</li>\n<li>Excellent organisational and communication skills, with the ability to guide cross-functional teams and drive project success.</li>\n<li>Problem-solving mindset, with the ability to adapt to changing project dynamics and implement effective solutions.</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":1793010257948},{"id":"job_8a7617b9-66f","title":"Senior CRA","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Turkey-Istanbul/Senior-Clinical-Research-Associate_JR157520","location":null,"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>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>","enriched_at":1793010254385},{"id":"job_71f20dfd-4d8","title":"Statistical Programmer (All Levels)","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/Statistical-Programmer_JR154337","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Data Science","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 Statistical Programmer at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and reporting.</p>\n<p>Your role will involve delivering statistical programming work to a high standard, working closely with your team and stakeholders.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Developing, validating, and maintaining complex statistical programs (SAS, R, &amp; similar) for data manipulation, analysis, and reporting in clinical trials.</li>\n<li>Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.</li>\n<li>Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.</li>\n<li>Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.</li>\n<li>Mentoring junior programmers and assisting in training team members on programming techniques and best practices.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Bachelor’s degree in statistics, mathematics, computer science, or a related field; advanced degree is a plus.</li>\n<li>5+ years experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming.</li>\n<li>Proficiency in programming languages SAS and R, along with exposure to Python and R Shiny with experience in clinical data management systems.</li>\n<li>Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently.</li>\n<li>Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members.</li>\n</ul>\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. 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":1793010253960},{"id":"job_8f27ee8d-c3f","title":"Principal Engineer II","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Chennai/Principal-Engineer-II_JR154115-1","location":"Chennai","job_type":"full-time","experience_level":"senior","work_arrangement":"hybrid","category":"Engineering","description":"<p>ICON is seeking a Principal Engineer II to join their Global Network Operations team. The successful candidate will serve as the highest technical escalation point, providing technical leadership, resolving complex network issues, supporting global infrastructure projects, and ensuring the stability, security, and availability of the enterprise network.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Act as the highest technical escalation point for critical network incidents and complex infrastructure issues</li>\n<li>Lead troubleshooting across multi-vendor enterprise network environments</li>\n<li>Perform root cause analysis (RCA) for major incidents and implement permanent corrective actions</li>\n<li>Provide technical guidance and mentorship to Level 1 and Level 2 engineers</li>\n<li>Participate in Major Incident Management (MIM) calls and lead technical recovery efforts</li>\n<li>Ensure the availability, stability, and performance of the global network infrastructure</li>\n<li>Support BAU operations involving routing, switching, firewalls, SD-WAN, load balancers, VPNs, DNS, and cloud networking</li>\n<li>Identify recurring operational issues and implement proactive improvements to reduce incidents</li>\n<li>Lead network implementation activities for global infrastructure projects</li>\n<li>Design, review, and implement network solutions in accordance with enterprise standards</li>\n<li>Support datacenter migrations, office deployments, cloud connectivity, and technology refresh initiatives</li>\n<li>Review implementation plans and provide technical approval for high-risk network changes</li>\n<li>Support mergers, acquisitions, and global expansion initiatives from a networking perspective</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>10+ years of hands-on enterprise networking experience</li>\n<li>Strong expertise in Cisco ACI, Fortinet Firewalls, NetScaler/F5 Load Balancers, SD-WAN technologies (preferably CATO), enterprise routing and switching, and cloud networking</li>\n<li>Strong analytical and problem-solving skills</li>\n<li>Ability to lead technical discussions and major incident calls</li>\n<li>Excellent communication and stakeholder management skills</li>\n<li>Ability to manage multiple priorities in a fast-paced global environment</li>\n<li>Strong documentation and presentation skills</li>\n<li>Self-motivated with the ability to work independently and mentor junior engineers</li>\n</ul>\n<p>Preferred Certifications:</p>\n<ul>\n<li>CCNP Enterprise or CCIE</li>\n<li>Fortinet NSE 7/NSE 8 or FCSS Network Security</li>\n<li>Citrix NetScaler Certification</li>\n<li>CATO Certified Professional</li>\n<li>AWS or Azure Networking Certification</li>\n<li>ITIL Foundation</li>\n</ul>\n<p>Rewards &amp; Benefits:</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":1793010250652},{"id":"job_0155a4ca-d41","title":"Senior Statistical Analyst","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Senior-Statistical-Analyst_JR158816","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Data Science","description":"<p>ICON is seeking a Senior Statistical Analyst to join its Real World Evidence (RWE) team. The successful candidate will work on observational research studies, real-world data analyses, health outcomes research, and epidemiology projects.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Support study conception, design, and protocol development for real-world evidence and observational research projects.</li>\n<li>Contribute to study start-up activities, including review and development of protocols, case report forms, and statistical methodologies.</li>\n<li>Write statistical methods sections of study protocols and develop statistical analysis plans.</li>\n<li>Perform sample size and power calculations.</li>\n<li>Review database specifications and participate in data review activities.</li>\n<li>Develop table, listing and figure shells and programming specifications.</li>\n<li>Lead the review and validation of raw and derived variables.</li>\n<li>Create and maintain derived datasets using SAS programming.</li>\n<li>Conduct statistical analyses using appropriate methodologies, including advanced and specialized statistical techniques.</li>\n<li>Develop and validate SAS programs, macros, tables, listings, figures, and project deliverables.</li>\n<li>Lead quality control activities throughout programming and analysis processes.</li>\n<li>Manage and review internal and external data transfers.</li>\n<li>Produce project reports, statistical outputs, visualizations, tables and graphs for client delivery.</li>\n<li>Contribute to manuscripts, abstracts, conference presentations and peer-reviewed publications.</li>\n<li>Write methods and results sections for final reports and scientific publications.</li>\n<li>Communicate directly with clients, investigators and cross-functional teams regarding project deliverables and statistical requirements.</li>\n<li>Represent Statistical Analysis in proposal development and RFP activities.</li>\n<li>Participate in department initiatives, process improvements, SOP development and training activities.</li>\n<li>Deliver internal technical presentations and contribute to knowledge sharing within the team.</li>\n<li>Attend departmental meetings and support broader Real World Evidence research activities.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Master&#39;s degree or PhD in Statistics, Biostatistics, Epidemiology, Mathematics, Data Science, Public Health, or a related quantitative discipline.</li>\n<li>Significant experience within the pharmaceutical, biotechnology, CRO, healthcare research, or Real World Evidence environment.</li>\n<li>Advanced SAS programming experience is essential, including development of datasets, statistical analyses, macros, tables, listings and figures.</li>\n<li>Strong understanding of statistical methodologies and their practical application to healthcare and observational data.</li>\n<li>Experience developing Statistical Analysis Plans (SAPs) and analysis specifications.</li>\n<li>Knowledge of observational study design, epidemiology, health outcomes research, registries, claims databases, electronic health records, or other real-world data sources is highly desirable.</li>\n<li>Experience applying statistical techniques such as regression modelling, survival analysis, repeated measures analysis and other advanced methods.</li>\n<li>Ability to independently manage statistical deliverables while collaborating effectively within multidisciplinary teams.</li>\n<li>Strong written and verbal communication skills with the ability to explain complex statistical concepts to both technical and non-technical audiences.</li>\n</ul>\n<p><strong>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":1793009583109},{"id":"job_a65fba0c-004","title":"Clinical Research Associate, China","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Beijing/Clinical-Research-Associate_JR158114-4","location":null,"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 Clinical Research Associate at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:</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<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:</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 organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</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":1793009302256},{"id":"job_58da3b3f-054","title":"Clinical Research Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Shanghai/Clinical-Research-Associate_JR158116-2","location":null,"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>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>","enriched_at":1793009299931}],"category_normalised":[{"category":"healthcare","count":55},{"category":"operations","count":2},{"category":"logistics & supply chain","count":2},{"category":"finance","count":2},{"category":"facilities & maintenance","count":2},{"category":"engineering","count":2},{"category":"data science","count":2},{"category":"sales","count":1},{"category":"customer service","count":1},{"category":"consulting","count":1}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":70}],"trend":"stable","wow_pct":0},"momentum":{"recent_14d":70,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":85036.5,"industry_median":null,"percentile":null,"sample_size":2,"by_region":[],"transparency_pct":3,"industry_transparency_pct":0,"transparency_warning":true},"market_share":{"company_jobs":70,"industry_total":70,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.216,"skill_weighted_score":0.247,"top_exposed_titles":[{"title":"Senior Medical Writer","count":2,"score":0.475},{"title":"Clinical Research Associate, China","count":2,"score":0.245},{"title":"Clinical Research Associate","count":2,"score":0.245}],"top_exposed_skills":[{"skill":"Medical Writing","count":3,"score":0.475},{"skill":"Project Management","count":3,"score":0.327},{"skill":"Data Analysis","count":6,"score":0.245},{"skill":"Clinical Trial Monitoring","count":6,"score":0.245},{"skill":"Communication Skills","count":5,"score":0.245},{"skill":"Organisational Skills","count":5,"score":0.245},{"skill":"Ich-gcp Guidelines","count":4,"score":0.245},{"skill":"Life Sciences","count":4,"score":0.203},{"skill":"Phlebotomy","count":3,"score":0.184},{"skill":"Communication","count":5,"score":0.149}]},"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"United States","count":7,"share_pct":43.8},{"region":"Unknown","count":2,"share_pct":12.5},{"region":"APAC","count":2,"share_pct":12.5},{"region":"India","count":2,"share_pct":12.5},{"region":"Canada","count":2,"share_pct":12.5},{"region":"Australia/NZ","count":1,"share_pct":6.3}],"emerging":[{"region":"United States","recent_30d":7,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":5,"exec_prior_90d_avg":0,"exec_growth_pct":100,"notable_exec_hires":[{"title":"Medical Director (Gastroenterology)","location":null,"posted_at":"2026-10-26"},{"title":"Director, Project Management","location":null,"posted_at":"2026-10-26"},{"title":"Sr Director, Project Delivery (Cardiovascular)","location":null,"posted_at":"2026-10-26"},{"title":"Facilities Director - Global CRU & Laboratory Facilities","location":null,"posted_at":"2026-10-26"},{"title":"Director IPH","location":null,"posted_at":"2026-10-25"}]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":0}}}}