• Own the full iOS release pipeline: CI/CD, TestFlight, and public/enterprise distribution. • Refactor legacy UIKit code toward modular, testable SwiftUI components where it adds value. • Profile, benchmark, and optimize memory, launch time, and frame rates. • Write unit & UI tests (XCTest, Snapshot testing) and comply to code-review standards with our tech lead. • Pair with design on motion/animation polish; pair with backend on GraphQL/REST contracts.

Senior CRA- Remote 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 We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic 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. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing: - Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. - Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. - Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. - Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. - Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: - Advanced degree in a relevant field such as life sciences, nursing, or medicine. - Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. - Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. - Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. - Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. - Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license - bilingual English and French Nous recherchons actuellement un(e) Senior Clinical Research Associate (CRA) pour rejoindre notre équipe diversifiée et dynamique. En tant que Senior CRA chez ICON Plc, vous jouerez un rôle essentiel dans la supervision et la gestion des activités des essais cliniques afin de garantir leur conformité aux protocoles, aux exigences réglementaires et aux normes de l’industrie. Vous contribuerez au succès des essais cliniques en assurant l’intégrité des données, la sécurité des participants et la conformité tout au long du cycle de vie de l’étude. Vos missions : - Assurer le suivi des sites d’essais cliniques afin de garantir le respect des protocoles d’étude, des exigences réglementaires et des Bonnes Pratiques Cliniques (BPC/GCP). - Effectuer des visites sur site pour évaluer la performance, résoudre les problèmes et apporter un soutien afin d’assurer la bonne exécution des essais. - Collaborer avec des équipes pluridisciplinaires pour garantir la collecte et le reporting des données dans les délais et avec précision. - Fournir formation et accompagnement au personnel des sites ainsi qu’aux autres CRAs afin de maintenir des standards élevés dans la conduite des essais cliniques. - Établir et entretenir des relations efficaces avec le personnel des sites et les parties prenantes afin de faciliter le bon déroulement des opérations. Votre profil : - Diplôme supérieur dans un domaine pertinent tel que les sciences de la vie, les soins infirmiers ou la médecine. - Expérience significative en tant que Clinical Research Associate, avec une solide compréhension des processus d’essais cliniques et des exigences réglementaires. - Capacité avérée à gérer simultanément plusieurs sites et projets, avec d’excellentes compétences organisationnelles et de résolution de problèmes. - Expertise en monitoring, en intégrité des données et en gestion de sites, avec une maîtrise des logiciels et outils d’essais cliniques. - Excellentes compétences en communication, relations interpersonnelles et gestion des parties prenantes, avec la capacité d’influencer et de garantir la conformité dans un environnement complexe. - Disponibilité pour des déplacements fréquents (au moins 60 % du temps, déplacements nationaux et internationaux – avion et voiture) et possession d’un permis de conduire valide. - Bilingue anglais / français. What ICON can offer you: 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, 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. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - 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. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

US, Senior Statistical Programmer 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 We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs, collaborating with biostatisticians, and ensuring compliance with regulatory standards. What You Will Be Doing: - Developing and validating SAS programs for statistical analysis and reporting of clinical trial data. - Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data. - Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting. - Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions. - Contributing to process improvements by identifying efficiencies in programming practices and methodologies. Your Profile: - Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field. - Experience in statistical programming, preferably in a clinical research or pharmaceutical setting. - Strong proficiency in SAS programming, with a solid understanding of statistical concepts and methodologies. - Excellent analytical and problem-solving skills, with a keen attention to detail. - Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information. What ICON can offer you: 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, 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. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - 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. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

We are hiring a Software Engineer at BlueCross BlueShield of Tennessee! In this role, you will design, build, and support data solutions that power targeted outreach campaigns for BlueCross BlueShield members. Your work will directly enable campaigns that help members receive timely, relevant information to support their health and care decisions. Day to day, you’ll work with large and diverse data sets, develop and maintain SQL- and Python-based solutions, support scheduled production jobs, and partner with business and technical teams to ensure accurate, reliable data flows into our campaign management systems. This role offers meaningful exposure to cloud migration efforts and the opportunity to learn and support end‑to‑end production processes that impact member engagement at scale. To be successful in this role, in addition to the core job requirements, you’ll bring strong SQL expertise, working knowledge of Python, and experience using Azure DevOps to manage and maintain code. You'll have experience deploying and supporting data solutions using CI/CD pipelines, ensuring reliable, repeatable, and auditable releases to production. You'll also have experience designing and implementing data quality control (QC) checks to validate completeness, accuracy, and consistency of data used in member outreach campaigns. You’ll be a strong candidate if you enjoy digging into data, understanding how it’s used by the business, and improving data quality and performance. Familiarity with analytics concepts and experience working in Google Cloud Platform (GCP) environments are nice-to-haves that can help accelerate ramp-up and impact on the team. Note: - Sponsorship is not available for this role. - This is a fully remote role, however, the final round of interviews will be conducted onsite at our Chattanooga, TN office. - Working hours are expected to align to Eastern Time. Job Responsibilities - Formulates and defines system scope and objectives through research and fact-finding to design, develop, modify, or integrate complex information systems. - Devises or modifies application systems and procedures to optimize functional requirements including capacity, operating time, response time, and form of desired results. - Designs, codes, tests, debugs, and documents programs, subroutines, and scripts. - May serve one or more project team roles, such as project lead, business systems analyst, or technical lead, for small to medium efforts or manage phases of medium to large efforts. - Maintains technical skill set for software languages, databases, platforms, operating systems, utilities and networks needed to support work assignments. - Responds to system failures and performance events by taking appropriate measures to reduce system downtime and eliminate recurrence of problems. - Regularly provides guidance and training to less-experienced analysts/programmers. Job Qualifications Education - Bachelors Degree in Computer Science or equivalent work experience required. Equivalent years of experience are determined as one year of technical experience for every year of college requested. Experience - 1 year - Experience with information technology concepts, application development methodology, terminology, and standards required - 3 years - Systems and programming experience required - 1 year - Expert working knowledge of at least one programming language in use at BCBST. Skills\Certifications - Proven skill with information technology in use at BCBST is required - Proven analysis, design, and coding skills, and demonstrated success in leading large and complex projects - Demonstrated ability to interpret and translate technical and/or or complex concepts into information meaningful to project team members and/or business personnel. - Be organized, reliable, and able to manage multiple tasks with exceptional work ethic. - Leadership skills - Must be able to communicate effectively with both technical and non-technical co-workers Number of Openings Available 1 Worker Type: Employee Company: BCBST BlueCross BlueShield of Tennessee, Inc. Applying for this job indicates your acknowledgement and understanding of the following statements: BCBST will recruit, hire, train and promote individuals in all job classifications without regard to race, religion, color, age, sex, national origin, citizenship, pregnancy, veteran status, sexual orientation, physical or mental disability, gender identity, or any other characteristic protected by applicable law. Further information regarding BCBST's EEO Policies/Notices may be found by reviewing the following page: BCBST's EEO Policies/Notices BlueCross BlueShield of Tennessee is not accepting unsolicited assistance from search firms for this employment opportunity. All resumes submitted by search firms to any employee at BlueCross BlueShield of Tennessee via-email, the Internet or any other method without a valid, written Direct Placement Agreement in place for this position from BlueCross BlueShield of Tennessee HR/Talent Acquisition will not be considered. No fee will be paid in the event the applicant is hired by BlueCross BlueShield of Tennessee as a result of the referral or through other means.