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The Product Specialist will provide day-to-day support for Enterprise Work Management products, including resolving incidents and managing service requests. They will also perform platform administration, document support procedures, and collaborate with vendors to resolve escalations.
The Technical Services Manager is responsible for managing high-standard operational services in MEP systems across the WPM portfolio to ensure efficient building performance. They will oversee planned and reactive Hard FM services, manage service partners, and ensure full compliance with health, safety, and legislative standards.
The HVAC Retrofit Sales Engineer will identify and develop new business opportunities for HVAC system replacements and energy efficiency upgrades. They will manage the full sales cycle from initial prospecting and site surveys to contract negotiation and project handover.
The developer will design, build, and maintain low-code business applications and dashboards to modernize U.S. Coast Guard mission processes. They will also engage directly with users during roadshows to capture requirements and develop rapid prototypes.
The Principal Software Engineer will design, develop, and implement Edifecs solutions for healthcare EDI transactions while providing technical leadership and mentorship to the development team. Responsibilities include configuring Edifecs tools, managing XEngine files, and leading agile development efforts in a cloud-based environment.
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The role involves managing trade architecture strategies to drive business growth and operational efficiency. You will be responsible for collaborating with cross-functional teams to implement trade management initiatives and support organizational goals.
The Business Development Manager is responsible for driving mortgage sales by building and maintaining relationships with top-tier mortgage brokers within a defined territory. They will provide training on bank products, ensure compliance with market conduct policies, and collaborate with internal teams to identify new business opportunities.
The auditor will independently plan and lead multimedia environmental compliance audits at government and commercial facilities nationwide. They are responsible for evaluating regulatory compliance, identifying risks, delivering technical findings, and providing practical recommendations to clients.
The Product Master Data Coordinator is responsible for maintaining the accuracy of data within the Material Master and managing incoming requests. They collaborate with various departments to ensure data integrity, resolve system errors, and support divisional needs for material updates.
Review eligibility for youth in care and prepare, file, and manage SSI-related applications, reviews, appeals, and payee changes. Coordinate with case workers, placements, and the Social Security Administration; maintain case records, provide reports and training, and support audits.
Provide technical, operational, educational, and sales support for cardiac rhythm management devices and therapies, including device checks, implant support, troubleshooting, documentation, and inventory coordination. Educate clinical customers, collaborate with sales teams, support customer and business needs, and travel extensively throughout the assigned territory.
The Regional Finance Manager will ensure financial governance, compliance, and operational excellence across multiple countries in the region. They will partner with leadership to provide financial insights, manage outsourced service providers, and drive process improvements.
The Senior Project Manager leads cross-functional teams to deliver Phase I-IV clinical trials from start-up through closeout. They are responsible for managing project timelines, budgets, and quality while serving as the primary point of contact for clients.
The Online Editor is responsible for managing the end-to-end production of educational videos, including pre-production, filming, and editing. They must collaborate with instructors and media producers to create innovative video content while maintaining high quality standards.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory documentation, investigational product accountability, and adverse event reporting. Guide and mentor CRA colleagues, support study planning and budgets, resolve site issues, and ensure compliance with protocols, ICH GCP, regulations, and SOPs.
Build relationships with medical experts and key opinion leaders, communicate scientific and clinical information about Alcon products, and gather external insights to inform company strategies. Support clinical trials and medical projects, provide medical information, address safety and product complaints, and collaborate with internal teams while maintaining regulatory and company compliance.
The Senior Clinical Project Manager oversees clinical research studies to ensure compliance with protocols, budgets, and regulatory standards. They serve as the primary sponsor contact while supervising clinical team members and managing study-specific functions like data management and pharmacovigilance.
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This position assesses patient clinical needs against established guidelines to ensure appropriate level of care and length of stay. It also coordinates care delivery across the continuum, monitors medical services, and advocates for members to ensure cost-effective, high-quality outcomes.
The Research Account Manager will own and drive territory growth by developing new business and expanding existing accounts through strategic planning and solution-based selling. They will act as the central point of orchestration for customer engagement, collaborating with technical and service teams to deliver integrated solutions.
The A/R Rep is responsible for billing, follow-up, claim edits, and provider enrollment review. They also handle cash posting, payer underpayment resolution, and various administrative or customer service functions.
The coordinator is responsible for managing inbound and outbound communications with patients and healthcare providers to facilitate therapy access. They must accurately document patient information in proprietary software and resolve inquiries while maintaining high standards of customer support.
The Sr. Technical Program Manager will lead the Consolidations program by coordinating multi-functional teams from planning through delivery. They are responsible for managing dependencies, tracking objectives and key results, and ensuring alignment across engineering, product, and business stakeholders.
The Research Computing Services Manager provides technical and financial oversight for non-desktop computing infrastructure to support biomedical research. They lead teams across Linux, Windows, database, and storage domains to ensure efficient, secure, and reliable research operations.
Perform preventative maintenance, DOT inspections, and mechanical repairs on light and medium-duty vehicles at customer locations. Document all findings and repairs accurately while maintaining compliance with safety and environmental regulations.
The agent provides administrative and operational support to maximize productivity, including data entry, processing, and database integrity verification. They also assist in producing reports, coordinating unit activities, and serving as a resource person for operational matters.
Lead end-to-end logistics and product distribution for small-molecule and biologics clinical and commercial programs, including temperature-controlled shipments, site-to-site movements, third-party providers, and domestic and international trade compliance. Develop logistics network and commercialization strategies, oversee provider performance and cross-functional projects, and drive compliant continuous improvement across the supply chain.
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The Business Development Manager is responsible for managing the entire sales cycle, from lead generation to closing, for the Resonant Clinical Solutions portfolio. This includes managing existing accounts, pursuing new target customers, and coordinating with internal teams to deliver customized solutions.
The Medical Science Liaison maximizes product value through high-quality scientific communication with leading specialists on a peer-to-peer basis. They are responsible for implementing the Medical Affairs Plan, providing scientific support to internal teams, and managing local clinical study activities.
The Account Manager II will develop and implement sales strategies to retain and grow accounts within an assigned territory while shadowing experienced staff. Responsibilities include identifying customer needs, conducting technical audits, and building professional relationships with key decision-makers.
The Senior Regulatory Affairs Specialist provides regulatory guidance to project teams and develops global regulatory strategies for new and existing medical devices. They are responsible for preparing regulatory submissions, ensuring compliance with health authority regulations, and supporting internal and external audits.
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