Role Description Core4ce is seeking an experienced Clinical Terminologist to support the Integrated Healthcare Transformation (IHT) initiative within the Veterans Health Administration (VHA). The Clinical Terminologist will serve as a subject matter expert in healthcare terminology, semantic interoperability, and clinical informatics, supporting the development and maintenance of standardized clinical data models and terminology mappings. This role requires a strong clinical background combined with deep expertise in terminology standards, ontology development, metadata management, and healthcare interoperability frameworks. The successful candidate will help ensure that clinical and benefits-related information is accurately represented, exchanged, and utilized across enterprise healthcare systems. - Develop, maintain, and optimize clinical terminology mappings and information models that support interoperability across healthcare systems and applications. - Map clinical and benefits-related concepts to industry-standard terminologies, including SNOMED CT, LOINC, RxNorm, FHIR, and other standards based on specific use cases and business requirements. - Design and maintain semantic infrastructure components, including metadata repositories, ontology models, controlled vocabularies, and terminology services. - Develop and manage domain-specific value sets, ensuring alignment with evolving clinical terminology standards and organizational requirements. - Monitor, evaluate, and implement updates to terminology standards and ensure appropriate incorporation into enterprise terminology management processes. - Collaborate with clinicians, informaticians, business stakeholders, and technical teams to define, model, and standardize healthcare data elements. - Support healthcare interoperability initiatives by ensuring consistent semantic representation across clinical systems, applications, and data exchanges. - Utilize terminology management tools to perform concept mapping, value set management, terminology maintenance, and semantic analysis. - Analyze clinical workflows, business processes, and use cases to identify terminology requirements and develop appropriate semantic solutions. - Participate in data governance and terminology governance activities to ensure compliance with enterprise standards and best practices. - Provide expertise in ontology development, metadata management, and semantic modeling to support healthcare modernization efforts. - Develop documentation, standards, procedures, and implementation guidance related to terminology management and interoperability. - Support quality assurance activities by validating terminology mappings, data definitions, and semantic models. - Collaborate with interdisciplinary teams, including physicians, nurses, pharmacists, disability specialists, allied health professionals, and benefits personnel, to ensure accurate representation of clinical and business concepts. - This position is designed to be flexible, with responsibilities evolving to meet business needs and enable individual growth. Qualifications - Must be able to obtain and maintain a Public Trust clearance. - Master's degree in Informatics, Computer Science, Health Informatics, Clinical Informatics, or a related field. - Certification in Informatics is required. - Minimum of 5 years of experience in clinical terminology management, semantic interoperability, healthcare informatics, or related disciplines. - Clinical background as a physician, nurse, pharmacist, or other allied health or healthcare-related professional. - Demonstrated expertise in healthcare terminology standards, including SNOMED CT, LOINC, RxNorm, FHIR, and other applicable interoperability standards. - Experience developing terminology mappings, semantic models, ontologies, metadata structures, and value sets. - Proficiency with terminology management tools and terminology services platforms. - Experience maintaining terminology content and implementing updates based on new or revised industry standards. - Strong understanding of healthcare data standards, interoperability frameworks, and clinical information systems. - Experience supporting semantic interoperability initiatives across complex healthcare environments. - Excellent analytical, problem-solving, communication, and stakeholder engagement skills. - Ability to translate complex clinical and technical concepts into standardized terminology models and data structures. Preferred Qualifications - Experience supporting Veterans Health Administration (VHA), Department of Veterans Affairs (VA), or other federal healthcare organizations. - Experience with disability-related terminology and benefits data standards. - Knowledge of healthcare data governance, master data management, and enterprise information architecture. - Experience supporting electronic health record (EHR) modernization initiatives. - Familiarity with HL7 standards, FHIR implementation guides, and healthcare information exchange frameworks. - Experience participating in terminology governance boards, standards organizations, or interoperability initiatives. Benefits - 401(k) with 100% company match on the first 6% deferred, with immediate vesting. - Comprehensive medical, dental, and vision coverage—employee portion paid 100% by Core4ce. - Unlimited access to training and certifications, with no pre-set cap on eligible professional development. - Tuition assistance for job-related degrees and courses. - Paid parental leave, PTO that grows with tenure, and generous holiday schedules. - The Forge gives every employee the chance to propose bold innovations and help bring them to life with internal backing.

Role Description Esta posición está ubicada en Medellín en la división Vascular (AVD). Abbott Vascular ofrece productos innovadores, mínimamente invasivos y costo efectivos para el tratamiento de enfermedades vasculares. - Promover, asesorar y capacitar al personal médico y asistencial en el manejo de productos y equipos de la compañía. - Dar soporte clínico a los procedimientos en las instituciones. - Generación de demanda del portafolio de productos en la zona a cargo. - Identificación de nuevas oportunidades de venta en clientes nuevos y existentes. - Gestionar la venta para lograr el presupuesto asignado. - Seguimiento a pedidos y requerimientos de productos para procedimientos. - Desarrollar y fortalecer las relaciones comerciales con los clientes. - Apoyar a marketing y ventas con la información relacionada con comportamiento de mercado. - Apoyar la gestión de inventarios de consignación, para solucionar posibles diferencias, optimizar la rotación de dispositivos, realizar seguimiento al producto con vencimiento corto y realizar proceso para evitar scrap. - Actualizar la información requerida de forma oportuna y acorde a las políticas vigentes en la plataforma Salesforce. - Reportar eventos adversos y/o reclamos presentados con los productos. - Acogerse al sistema de calidad corporativo. - Realizar otras funciones asignadas que permitan mantener un buen desempeño y el logro de los objetivos. Qualifications - Profesional en Enfermería o en Instrumentación Quirúrgica. Requirements - Profesional en Enfermería o en Instrumentación Quirúrgica. Benefits - Desarrollo profesional con una empresa internacional donde podrás hacer crecer la carrera que sueñas. - Una compañía reconocida como mejor lugar para trabajar en docenas de países alrededor del mundo y nombrada una de las empresas más admiradas del mundo por Fortune. - Una compañía que es reconocida como una de las mejores compañías grandes para trabajar, así como un mejor lugar para trabajar para la diversidad, las madres trabajadoras, mujeres ejecutivas y científicas.

Role Description The Clinical Research Regulatory Specialist will collaborate with OneR operations team and OneOncology practices to support clinical research across the OneOncology network. This role will play a crucial part in ensuring compliance with regulatory requirements and guidelines for our clinical research projects. The Clinical Research Regulatory Specialist will work closely with cross-functional teams to facilitate the regulatory aspects of clinical trials, ensuring smooth and efficient processes from study initiation through to completion. Additionally, they will engage with various practices within our network to streamline regulatory processes and foster collaboration. Responsibilities - Ensure adherence to all relevant regulatory requirements, including FDA regulations, ICH guidelines, and local regulatory requirements. - Prepare, submit, and maintain regulatory documents, such as investigational new drug (IND) applications, amendments, and annual reports. - Coordinate regulatory submissions to regulatory authorities and ethics committees, ensuring timely and accurate completion. - Assist in the review of clinical trial protocols, informed consent forms, and other study-related documents to ensure compliance with regulatory standards. - Review and modify study specific informed consent forms for readability, clarification of payments, costs, and standard of care language, and to ensure that all elements required by the Food and Drug Administration (FDA) are included. - Prepare, route, and submit essential regulatory documents to sponsors/CROs on behalf of network practices. - Collaborate with investigators and study teams to address regulatory issues and provide guidance on regulatory requirements. - Coordinate regulatory activities during study start-up, including obtaining regulatory approvals, organizing regulatory binders, and ensuring site compliance with regulatory requirements. - Maintain accurate and up-to-date regulatory files and documentation, ensuring completeness and compliance with regulatory standards. - Establish and maintain an electronic regulatory binder system to securely store and manage regulatory documents and submissions. - Track and communicate regulatory submission timelines, milestones, and status updates to internal stakeholders. - Provide training and support to study teams and investigators on regulatory requirements, procedures, and best practices. - Stay informed about changes in regulatory requirements and industry standards, and disseminate relevant information to team members. - Cultivate and maintain relationships with various practices within our network to streamline regulatory processes and promote collaboration. - Other duties as assigned to help drive our mission of improving the lives of everyone living with cancer. Qualifications - Bachelor's degree in a relevant field (e.g., life sciences, pharmacy, nursing) required; advanced degree preferred. - Minimum of 1-2 years of experience in clinical research, with a focus on regulatory affairs and compliance. - Proficiency in Microsoft Office applications and familiarity with electronic data capture (EDC) systems, electronic regulatory binder system, and clinical trial management systems (CTMS) preferred. - Certification in clinical research (e.g., SoCRA, ACRP) is a plus. Key Competencies - Strong understanding of clinical trial processes, regulatory requirements (e.g., ICH-GCP, FDA guidelines), and industry standards. - Exceptional attention to detail and organizational skills. - Effective communication and interpersonal skills, with the ability to collaborate across multidisciplinary teams. - Ability to work independently and collaboratively in a fast-paced environment.

Role Description The Senior Product Analyst – Digital Transformation (CRO) plays a critical role in advancing SCRI’s digital strategy by translating business priorities into actionable solutions. Serving as the bridge between business stakeholders and IT delivery teams, this role drives operational excellence, data integrity, and innovation at SCRI Development Innovations, a Contract Research Organization (CRO). A key focus is shaping and enabling AI-driven transformation opportunities that deliver measurable business outcomes, with a strong emphasis on hands-on delivery, rapid experimentation, and learning-by-doing through applied digital and AI solutions. Duties & Responsibilities - Partner with business and IT teams to gather, document, and prioritize requirements, while owning end-to-end problem discovery through pilot delivery for assigned initiatives. - Participate in cross-functional workshops to identify AI-enabled use cases and iteratively build prototypes, actively configuring, testing, and refining solutions hands-on. - Translate strategy into user stories, workflows, and specifications for process optimization, and contribute directly to backlog refinement, release planning, and UAT. - Ensure solutions align with enterprise data strategy, integration needs, 21 CFR Part 11 requirements and responsible AI practices. - Support change management, documentation, and user enablement for sustainable adoption. - Document reusable patterns, playbooks, and AI/automation components to accelerate future initiatives and organizational learning. Qualifications - 3-5+ years in product or business analysis within dynamic digital transformation environments. - Demonstrated success supporting healthcare or life sciences product initiatives. - Ability to rapidly learn new business domains and processes to build strong partnerships. - Proven track record driving technology adoption and identifying high-value AI opportunities, including directly building or piloting solutions. - Strong analytical skills with experience reporting progress and outcomes to leadership. - Experience building low/no-code or AI-enabled proof-of-concept solutions to validate ideas before scale, with personal ownership of prototypes, pilots, or MVPs. Requirements - Knowledge of Agile, SDLC, and regulatory considerations in clinical research environments (21 CFR Part 11). - Awareness of data governance, interoperability standards, and digital adoption analytics. - Familiarity with coding principles, AI Agentic/automation tools (hands-on preferred), APIs, with the ability to independently configure and test solutions. - Knowledge of AWS, Azure, and modern research applications vendors such as Veeva, Medidata, Oracle, etc. - Ability to do hands-on POC with AI tools, ROI analysis for product initiatives, and iterate based on real user and system feedback. Skills - Advanced analytical and problem-solving skills to identify business problems, define solution options, and consult with stakeholders to deliver impactful outcomes. - Proficiency with Microsoft Copilot, AI Agents, and project management tools e.g., Jira, Confluence, Planview, Smartsheets. - Strong communication skills to translate business needs into clear technical requirements and simplify technical concepts for business stakeholders, while influencing decisions and achieving alignment. - Skilled in requirements traceability, validation, and driving cross-functional alignment. - Experience using process-mining and workflow analysis to uncover automation opportunities, and rapidly test those opportunities through prototypes or pilots. Benefits - Comprehensive benefits to support physical, mental, and financial well-being. - Competitive compensation package determined by performance, experience, skills, equity, and geographical markets. - Annual bonus or long-term incentive opportunities may be offered. Company Description Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.