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As a Senior CRA, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p>Your Profile:</p>\n<ul>\n<li>Advanced degree in a relevant field such as life sciences, nursing, or medicine.</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements (7+ years&#39; minimum required).</li>\n<li>At least 2 years&#39; experience working on Oncology studies.</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>Ability to travel at least 60% of the time (international and domestic) and possess a valid driver&#39;s license.</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":1793014288360},{"id":"job_16022982-5ea","title":"Senior Statistical Programmer - Client Based","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/South-Africa-Johannesburg/Senior-Statistical-Programmer_JR145439","location":null,"job_type":null,"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.</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>We&#39;re looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward-thinking team. At ICON, you&#39;ll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision-making in global healthcare.</p>\n<p>In this role, you&#39;ll take ownership of developing and validating high-quality statistical programs, partnering closely with expert biostatisticians, and ensuring our outputs meet the highest scientific and regulatory standards. Your expertise will directly support the success of our clinical studies and the advancement of life-changing therapies.</p>\n<h4>What You Will Be Doing</h4>\n<ul>\n<li>Designing, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.</li>\n<li>Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.</li>\n<li>Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.</li>\n<li>Supporting the creation of statistical reports, presentations, and regulatory submission documentation.</li>\n<li>Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team.</li>\n</ul>\n<h4>Your Profile</h4>\n<ul>\n<li>Bachelor&#39;s or Master&#39;s degree in Statistics, Mathematics, Computer Science, or a related discipline.</li>\n<li>Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry.</li>\n<li>Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.</li>\n<li>Exceptional analytical and problem-solving abilities, with meticulous attention to detail.</li>\n<li>Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.</li>\n</ul>\n<h4>Rewards &amp; Benefits</h4>\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":1793014286506},{"id":"job_08f5c72f-9d9","title":"Sr. Clinical Research Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Spain-Madrid/Sr-Clinical-research-Associate_JR144790","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>ICON is seeking a Senior Clinical Research Associate (CRA) to join their team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p><strong>Responsibilities:</strong></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<ul>\n<li>Advanced degree in a relevant field such as life sciences, nursing, or medicine.</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>Ability to travel at least 60% of the time (international and domestic).</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":1793014284180},{"id":"job_6aad05e9-74f","title":"Lead Clinical Data Science Programmer","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/Lead-Clinical-Data-Science-Programmer_JR134948","location":"Bangalore, India","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.</p>\n<p>As a Lead Clinical Data Science Programmer at ICON Strategic Solutions, you will be instrumental in leading the development and implementation of advanced data science solutions for clinical trials. Your role will involve overseeing data programming activities, data pipeline maintenance, and generating visualized output analysis to support clinical research and decision-making.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Be responsible for delivery in a continuous improvement framework with respect to systems deployment, life cycle management and enhancements supported user groups.</li>\n<li>Contribute to initiatives to yield faster and more effective report development, efficient change management services for analytics platforms.</li>\n<li>Use your technical expertise with clinical data and report building, and experience gained through working with diverse and complex business processes and associated system infrastructures.</li>\n<li>Work in a matrix environment across functions and departments.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>More than 4 years’ experience as a Business Analyst, working within Data Warehouse platforms in a regulated industry within a clinical trial environment.</li>\n<li>In-depth knowledge of Python and its associated data manipulation packages.</li>\n<li>Advanced knowledge of SDTM data structures.</li>\n<li>Knowledge to gather requirements and writing user requirement documentation.</li>\n<li>Ability to work independently on assignments of moderate to high complexity without support.</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":1793014093466},{"id":"job_8bb84a68-9aa","title":"Senior Statistical Programmer","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Romania-Bucharest/Principal-Programmer_JR145561-1","location":null,"job_type":null,"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 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>At ICON, we’re looking for a Senior Statistical Programmer who is ready to do more than just write code, you will help bring clinical research to life. You will join a collaborative, diverse team working on studies that genuinely matter, where your expertise helps turn complex data into clear insights that shape medical advancements.</p>\n<p>If you enjoy solving problems, working closely with experts across disciplines, and seeing the tangible impact of your work, this could be the role for you.</p>\n<h4>What You’ll Be Doing</h4>\n<ul>\n<li>Building impactful solutions – Develop, validate, and maintain complex statistical programs (primarily in R) to support data analysis and reporting for clinical trials.</li>\n<li>Leading from the front – Take ownership of one or more studies, working alongside Principal Programmers and acting as a key contact for a leading FSP sponsor.</li>\n<li>Collaborating across teams – Partner closely with biostatisticians and cross-functional colleagues to translate study requirements into robust, accurate statistical outputs.</li>\n<li>Shaping analysis strategy – Prepare and review statistical analysis plans (SAPs), programming specs, and derived datasets to meet regulatory expectations.</li>\n<li>Ensuring quality and compliance – Safeguard data integrity and adhere to industry standards (ICH/GCP) throughout the programming lifecycle.</li>\n<li>Supporting others to grow – Mentor junior programmers and contribute to building a culture of knowledge-sharing and continuous improvement.</li>\n</ul>\n<h4>What You Bring</h4>\n<ul>\n<li>A degree in statistics, mathematics, computer science, or a related field (postgraduate qualifications are a bonus).</li>\n<li>Solid experience as a statistical programmer within clinical research.</li>\n<li>Strong hands-on expertise in R programming (ideally 5+ years in a clinical trials setting).</li>\n<li>A sharp analytical mindset, attention to detail, and confidence working independently.</li>\n<li>The ability to explain complex statistical concepts in a clear, accessible way,and collaborate effectively with both technical and non-technical stakeholders.</li>\n</ul>\n<h4>Why ICON?</h4>\n<p>At ICON, your work isn’t just technical, it’s meaningful. You’ll contribute to research that improves lives, while working in an environment that values collaboration, innovation, and growth. Whether you’re leading studies or mentoring others, you’ll have the support and autonomy to make a real difference.</p>\n<h4>Rewards &amp; Benefits</h4>\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":1793014092460},{"id":"job_11d29fa0-510","title":"Project Manager, FSA","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Shanghai/Project-Manager--FSA_JR146033-1","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 Project Manager, FSA at ICON, you will be responsible for planning and managing Feasibility and Site Activation (FSA) activities for assigned clinical studies. You will work cross-functionally to deliver timely, high-quality start-up while maintaining strong communication with customers and internal stakeholders.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Developing and managing FSA project plans, timelines, and deliverables for assigned studies.</li>\n<li>Coordinating feasibility assessments, country and site recommendations, and start-up strategies in collaboration with functional experts.</li>\n<li>Overseeing essential document collection, ethics and regulatory submissions, and site activation milestones.</li>\n<li>Tracking progress against timelines and KPIs, proactively identifying risks and implementing mitigation plans.</li>\n<li>Serving as the primary FSA contact for internal teams and customers for study-level start-up matters.</li>\n<li>Contributing to process improvement and best practice sharing within the FSA project management team.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences, healthcare, business, or a related field, or equivalent experience.</li>\n<li>Strong experience in clinical research with a focus on feasibility, site activation, or start-up project management.</li>\n<li>Proven ability to manage project plans, timelines, and cross-functional coordination in a fast-paced environment.</li>\n<li>Good understanding of regulatory, ethics, and contractual requirements affecting study start-up.</li>\n<li>Excellent communication, organisational, and stakeholder management skills.</li>\n<li>Detail-oriented and proactive, with a commitment to quality, predictability, and customer satisfaction.</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":1793014087906},{"id":"job_92e95e61-96f","title":"Project Manager, Japan","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Japan-Tokyo/Project-Manager_JR148243","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Operations","description":"<p>ICON is seeking a Project Manager to join their team in Japan. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.</li>\n<li>Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration.</li>\n<li>Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track.</li>\n<li>Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organisational objectives.</li>\n<li>Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor’s degree in project management, business, or a related field is preferred, with significant experience in project management and team leadership.</li>\n<li>Proven track record of successfully managing projects from inception to completion, with a focus on delivering results within scope, time, and budget constraints.</li>\n<li>Strong leadership and organisational skills, with the ability to effectively manage project teams and prioritise tasks.</li>\n<li>Excellent communication and interpersonal skills, with the ability to build relationships and manage stakeholder expectations.</li>\n<li>Proficiency in project management tools and methodologies, with certifications such as PMP or PRINCE2 being advantageous.</li>\n<li>Detail-oriented, proactive, and adaptable, with a commitment to achieving project goals and driving continuous improvement.</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":1793014086906},{"id":"job_2194d03c-590","title":"Clinical Dietary Aide","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Lenexa-KCI-PRA/Clinical-Dietary-Aide_JR147286","location":null,"job_type":null,"experience_level":null,"work_arrangement":"onsite","category":"Healthcare","description":"<p>ICON is seeking a Clinical Dietary Aide to support meal service operations within its clinical research unit. As a Clinical Dietary Aide, you will help ensure that clinical trial participants receive meals and snacks safely, accurately, and on schedule. This includes preparing meal areas, delivering trays, maintaining kitchen and dining spaces, and providing friendly, patient-focused service throughout their stay.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Preparing, stocking, and maintaining kitchen, cafeteria, and dining areas in accordance with safety, cleanliness, and food-handling standards.</li>\n<li>Setting up trays, utensils, beverages, and supplies needed for meal service.</li>\n<li>Delivering meals and snacks to clinical trial participants according to dietary requirements and study schedules.</li>\n<li>Ensuring accurate labeling, portioning, and timing of meals based on protocol guidelines.</li>\n<li>Assisting with cleanup, including counters, equipment, dishes, carts, and dining areas.</li>\n<li>Working with clinical staff to coordinate meal timing around study procedures or restrictions.</li>\n<li>Providing excellent customer service to participants to ensure a comfortable and positive dining experience.</li>\n<li>Reporting participant needs or concerns promptly to the clinical team.</li>\n<li>Supporting general clinic operations with light administrative or participant-support tasks as needed.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Experience in dietary aide, food service, hospitality, senior living, or customer service roles.</li>\n<li>Strong attention to cleanliness, organization, and food-safety procedures.</li>\n<li>Excellent communication, teamwork, and customer service skills.</li>\n<li>Ability to multitask and work efficiently in a fast-paced environment.</li>\n<li>Professional, reliable, and comfortable interacting with clinical trial participants.</li>\n<li>Willingness to support flexible scheduling needs based on study activities.</li>\n<li>No previous clinical experience required , training provided.</li>\n</ul>\n<p><strong>Why Join ICON?</strong></p>\n<ul>\n<li>Be part of a mission-driven team supporting clinical trials that advance patient health.</li>\n<li>Gain exposure to the clinical research field with opportunities to learn and grow.</li>\n<li>Supportive team environment with training provided for all responsibilities.</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":1793013385048},{"id":"job_3391f709-e64","title":"CRA II","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Spain-Madrid/Clinical-Research-Associate-II_JR146918","location":null,"job_type":"full-time","experience_level":"mid","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 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 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>Responsibilities</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 organisational 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<li>Good level of English.</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. 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":1793013383737},{"id":"job_ccd63ba1-e28","title":"Clinical Research Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Clinical-Research-Associate_JR141958","location":null,"job_type":"full-time","experience_level":"mid","work_arrangement":null,"category":"Healthcare","description":"<p>ICON is seeking a Clinical Research Associate II to join their 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>Responsibilities</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 organisational 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) and possess a valid driver&#39;s license.</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":1793013382973}],"category_normalised":[{"category":"healthcare","count":74},{"category":"data science","count":5},{"category":"finance","count":4},{"category":"operations","count":3},{"category":"logistics & supply chain","count":3},{"category":"engineering","count":3},{"category":"sales","count":2},{"category":"facilities & maintenance","count":2},{"category":"customer service","count":1},{"category":"consulting","count":1}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":98}],"trend":"stable","wow_pct":0},"momentum":{"recent_14d":98,"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":2,"industry_transparency_pct":0,"transparency_warning":true},"market_share":{"company_jobs":98,"industry_total":98,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.237,"skill_weighted_score":0.294,"top_exposed_titles":[{"title":"Clinical Research Associate, China","count":5,"score":0.245},{"title":"Clinical Research Associate","count":3,"score":0.245},{"title":"Senior Medical Writer","count":2,"score":0.475},{"title":"Principal Medical Writer","count":2,"score":0.475},{"title":"Clinical Research Associate II","count":2,"score":0.245}],"top_exposed_skills":[{"skill":"Statistics","count":3,"score":0.567},{"skill":"Mathematics","count":3,"score":0.567},{"skill":"Medical Writing","count":4,"score":0.475},{"skill":"Data Analysis","count":7,"score":0.245},{"skill":"Clinical Trial Monitoring","count":8,"score":0.245},{"skill":"Communication Skills","count":8,"score":0.245},{"skill":"Organisational Skills","count":7,"score":0.245},{"skill":"Good Clinical Practice GCP","count":6,"score":0.245},{"skill":"Data Integrity","count":6,"score":0.245},{"skill":"Site Management","count":6,"score":0.245}]},"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"United States","count":7,"share_pct":31.8},{"region":"India","count":4,"share_pct":18.2},{"region":"Unknown","count":3,"share_pct":13.6},{"region":"APAC","count":3,"share_pct":13.6},{"region":"Canada","count":2,"share_pct":9.1},{"region":"EU","count":2,"share_pct":9.1},{"region":"Australia/NZ","count":1,"share_pct":4.5}],"emerging":[{"region":"United States","recent_30d":7,"prior_30d":0,"growth_pct":100},{"region":"India","recent_30d":4,"prior_30d":0,"growth_pct":100},{"region":"Unknown","recent_30d":3,"prior_30d":0,"growth_pct":100},{"region":"APAC","recent_30d":3,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":7,"exec_prior_90d_avg":0,"exec_growth_pct":100,"notable_exec_hires":[{"title":"Vice President, Internal Audit","location":"Dublin","posted_at":"2026-10-26"},{"title":"BD Sr. Director","location":null,"posted_at":"2026-10-26"},{"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"}]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":0}}}}