Jobs at Triad Financial Services, Inc.

The Senior Pipe Stress Engineer role supports the Sentinel Program, a critical modernization effort for the U.S. nuclear deterrent infrastructure. Based in Ogden, Utah, this full-time position requires US citizenship and involves performing detailed pipe stress analysis using AutoPipe software in compliance with ASME B31.3 and B31.1 codes. Key responsibilities include modeling piping systems to verify flexibility and stability, coordinating with layout and support engineering teams, and resolving complex design conflicts. The position offers the opportunity to work on high-impact national security projects within a collaborative engineering environment. The role is fully onsite and requires a bachelor's degree with significant relevant experience.

This full-time Acquisition Program Analyst role serves as a Subject Matter Expert supporting Fighter Modernization programs at the Pentagon. The position involves managing a $10 billion portfolio of global power initiatives, including legacy and next-generation aircraft and munitions. Key responsibilities include supporting budget preparation and defense, analyzing program execution data, and providing strategic recommendations on acquisition strategies and milestone decisions. The role requires maintaining compliance with complex Air Force policies and preparing documentation for high-level reviews and congressional activities. This opportunity appeals to professionals seeking to directly influence the future of Air Force combat capabilities within a collaborative headquarters environment. The position is onsite at the Pentagon and offers a comprehensive benefits package including health insurance, retirement matching, and paid time off.

This full-time Licensed Practical Nurse role supports the medical-surgical unit at Cone Health during night shifts. The position involves delivering direct bedside care, administering medications, and monitoring adult patients while collaborating with RNs and providers to ensure safe, high-quality treatment. Key responsibilities include performing patient assessments, documenting changes in condition using EMR systems, and educating patients and families on care plans. The role appeals to candidates seeking a supportive, inclusive culture with robust professional development opportunities to grow their med-surg skills within the Piedmont Triad community. This position requires an active LPN license and BLS certification, offering a stable environment for those dedicated to compassionate patient care.

The Supervisor, Fulfillment role is an onsite leadership position based in Raleigh, North Carolina, within Millennium Print Group, a leading manufacturer of trading card games. The role involves overseeing daily warehouse operations including shipping, receiving, and order processing while ensuring high standards for quality, safety, and on-time delivery. Key responsibilities include managing and mentoring fulfillment staff, monitoring operational performance, and driving continuous improvement initiatives in partnership with department leadership. This position appeals to candidates seeking to join a rapidly growing, forward-thinking organization where their work directly supports globally recognized products. The role offers a collaborative culture focused on operational excellence and provides significant opportunities for professional growth within a high-performing team.

The Engineering Automation Supervisor role leads a team of automation engineers within Bechtel's Infrastructure division, specifically supporting the U.S. Air Force Sentinel Program's ground-based strategic deterrent project in Ogden, Utah. Key responsibilities include supervising engineering assignments, coordinating digital engineering workflows across disciplines, and managing the Integrated Digital Environment to ensure data compliance and model accuracy. The position requires overseeing BIM content libraries, facilitating design reviews, and aligning project delivery with strict government standards. This opportunity appeals to candidates seeking to work on high-impact national security infrastructure while fostering an inclusive culture that values continuous improvement and professional growth within a global, diverse organization.

This full-time 3D CAD Specialist role is based in Ogden, Utah, within the Engineering Automation and Digital Delivery team supporting the high-profile Sentinel Program. The position focuses on integrating customer solids models with Building Information Modeling software to support engineering contract deliverables. Key responsibilities include translating and coordinating BIM data into Siemens NX formats, managing model exchanges with stakeholders, and developing documentation for modeling processes. The role appeals to candidates seeking to work on critical national infrastructure projects with a global leader known for its collaborative culture and commitment to sustainable growth. The position requires on-site presence and offers opportunities to coach engineering teams and interface with cross-functional departments.

This IT Security Intern role supports the corporate Support Center at Atria Senior Living by assisting with daily information security operations. The intern works under the guidance of the IT Security team to monitor security systems, triage incidents, and analyze potential threats like phishing emails. Key responsibilities include maintaining security documentation, supporting Security Operations Center workflows, and tracking vulnerability remediation efforts. The position offers hands-on exposure to core cybersecurity tools and best practices, providing a strong foundation for a future career in the field. The role is appealing due to the supportive work environment, opportunities for professional advancement, and a culture that promotes work-life balance. This is an on-site internship designed for students actively pursuing a degree in a related technical field.

This per diem role as a Discharge Planning Coordinator supports the Continuum of Care team in facilitating patient transitions from hospital to home or post-acute facilities. The position involves coordinating with case managers and social workers to ensure smooth discharge communication, reviewing post-acute referrals, and conducting follow-up calls to discharged patients. Key duties include arranging transportation and durable medical equipment, communicating with external providers, and documenting care plans in the electronic medical record. The role appeals to Licensed Vocational Nurses seeking a collaborative environment where they can directly impact patient continuity of care. The position offers flexible scheduling with 8-hour day shifts, requires floating between hospital locations, and includes weekend and on-call coverage.

This full-time Product Engineer role at Triad Technologies supports the sealing products division within the Ohio region, primarily serving Cleveland and Cincinnati. The position combines technical expertise with customer relationship management to drive sales growth by providing engineered solutions for sealing technologies. Key responsibilities include acting as a trusted technical advisor for seal selection and application, conducting on-site troubleshooting and failure analysis, and collaborating with sales teams to develop growth strategies. The role is appealing for its opportunity to work directly with customers in a hands-on capacity, fostering strong professional relationships while solving complex mechanical challenges. The position requires approximately 40% travel for in-person support and is based on a standard Monday through Friday schedule.

The Trial Attorney II role within the Chief Disciplinary Counsel department in Houston represents the Texas Commission for Lawyer Discipline during attorney disciplinary proceedings. Key responsibilities include presenting cases before District Grievance Committees, District Courts, and the Board of Disciplinary Appeals while maintaining frequent contact with State Bar departments and outside agencies. This position offers the opportunity to serve the public interest by upholding professional standards within the legal community. The role is based on-site in Houston and involves regular interaction with various legal entities and organizations.

The Clinical Trial Laboratory Coordinator role supports the Division of Clinical Research at UT MD Anderson, a leading cancer research institution. This position focuses on ensuring high-quality protocol execution and regulatory compliance within laboratory operations. Key responsibilities include managing specimen collection, processing, and shipment logistics while utilizing the LIMS system for documentation. The coordinator also oversees clinical trial inventory, leads protocol implementation, and facilitates collaboration between laboratory staff, study teams, and sponsors. The role is appealing for its opportunity to contribute to groundbreaking cancer research within a mission-driven environment that prioritizes patient safety and scientific advancement. The position offers a hybrid work arrangement and supports professional growth through access to extensive institutional resources and a collaborative culture.

The Senior Trial Attorney role at Redmann Law involves leading complex litigation cases from pre-trial preparation through appeals and potential jury trials. Key responsibilities include managing a substantial caseload, representing clients in court, and providing mentorship to junior attorneys on conflict resolution and legal strategies. The position is based in New Orleans, Louisiana, and offers a collaborative environment within a firm dedicated to empowering clients with over three decades of experience. This opportunity appeals to experienced litigators seeking a challenging yet fulfilling setting where they can utilize their leadership skills and contribute to a team focused on achieving fair legal outcomes.

The Post Trial Access Manager role within IQVIA's clinical research division is responsible for executing global programs that provide investigational products to patients after clinical trials conclude but before regulatory approval. Key duties include developing program timelines and budgets, ensuring compliance with international regulatory frameworks, and leading cross-functional teams to manage supply strategies and vendor contracts. The position offers the opportunity to work in a dynamic global environment where professionals can drive patient access to life-saving therapies while advancing their expertise in pre-approval access mechanisms. The role supports a mission to improve patient outcomes through innovative medical treatments and requires minimal supervision to manage complex, multi-regional initiatives.

The University of Maryland School of Medicine seeks an Associate Professor or Professor to serve as the inaugural Director of the Data Coordinating Center and Clinical Trial Epidemiologist. This faculty role involves leading the development of a new institutional hub that unifies clinical research coordination, data management, and quantitative support across the campus. Key responsibilities include providing scientific and operational leadership for multidisciplinary teams, designing and executing multisite clinical trials, and securing extramural funding to sustain a competitive research program. The position offers the unique opportunity to shape the future of clinical trial infrastructure at a leading academic medical center while engaging in teaching and mentoring graduate and medical students. The role is based on-site in Baltimore and includes a comprehensive benefits package with significant leave and professional development resources.

The Clinical Trial Liaison role at ICON plc is a field-based position focused on supporting clinical trials by bridging the gap between sponsors and research sites. The individual acts as a site engagement specialist, providing scientific and clinical guidance to investigators while developing strategies to optimize patient enrollment. Key responsibilities include cultivating relationships with key stakeholders, translating best practices into local actions, and utilizing a strong medical network to recruit appropriate trial sites. This position appeals to candidates seeking a dynamic career in a diverse, inclusive culture that rewards high performance and nurtures talent. The role offers flexibility with a home or office base, though it requires significant national and international travel to engage with sites and attend industry conferences.

The Clinical Trial Support Assistant role is an onsite, full-time position based in Indianapolis, IN, providing operational support to teams managing investigation materials and clinical supply workflows. Key responsibilities include inputting and updating study supply data with high accuracy, reviewing and organizing material-related documents, tracking communications, and generating reports to monitor study activity. The position also involves maintaining electronic records, assisting with study closeout tasks, and supporting system troubleshooting. This role appeals to detail-oriented professionals seeking to develop expertise in clinical supply systems within a collaborative environment. The company offers comprehensive benefits including medical, dental, vision, paid time off, and a 401(k) plan with employer matching. The work arrangement requires on-site presence during standard business hours with occasional overtime.

The Clinical Trial Assistant role supports the execution of clinical studies within Scout Clinical, a leader in patient reimbursement and trial logistics. This position collaborates closely with project management teams to ensure operational excellence throughout the study lifecycle. Key responsibilities include coordinating study activities, maintaining project calendars, managing documentation, and configuring user access within the company portal. The role also involves handling client communications, processing invoices, and distributing virtual payments. The position appeals to candidates seeking a fast-paced environment with a culture focused on innovation and making complex processes easier. It offers opportunities for professional growth within a rapidly expanding team and requires strong organizational skills and attention to detail.

The Clinical Trial Monitor II role within the Clinical Trials Office at Dana-Farber Cancer Institute ensures research compliance with federal regulations and institutional policies. Key responsibilities include conducting remote data reviews and onsite monitoring visits to verify data accuracy, developing monitoring plans, and mentoring new team members. The position requires managing multiple projects simultaneously while promoting a culture of regulatory awareness. This opportunity appeals to professionals seeking to contribute to groundbreaking cancer research within an inclusive, mission-driven academic environment. The role is based in Boston with occasional travel required for onsite visits.

This part-time Clinical Trial Assistant role supports Lumicell's Clinical Affairs organization within a mission-driven startup focused on revolutionizing cancer surgery. The position involves preparing meeting materials, managing action item trackers, and coordinating cross-functional efforts between Clinical, Regulatory, and Medical Affairs teams. Key responsibilities include maintaining Clinical Trial Management Software and electronic Trial Master Files, ensuring documentation compliance, and supporting site engagement activities. The role appeals to candidates seeking flexible hours of 20 to 25 per week while contributing to groundbreaking work in breast cancer treatment. It offers the opportunity to work in a collaborative, high-performing environment with a diverse and inclusive culture.

This full-time Legal Assistant role supports the trial and litigation team at Clyde & Co US LLP, focusing on high-volume complex legal document preparation and court filing. Key responsibilities include managing attorney calendars, filing pleadings in state and federal courts, assisting with trial logistics, and handling administrative tasks such as billing and expense reporting. The position requires five years of litigation experience and proficiency with electronic filing systems. The role is appealing due to the firm's hybrid work flexibility, comprehensive benefits including generous paid time off and parental leave, and a strong commitment to professional growth through mentorship and global training programs. Candidates join a diverse, inclusive environment with a global presence and a focus on community service.

This full-time Certified Medical Assistant role supports clinical operations within a physician practice at Hackensack Meridian Health. The position involves preparing exam rooms, recording patient vital signs, and performing specialized procedures such as EKGs, phlebotomy, and lab testing under professional supervision. Key responsibilities also include maintaining accurate patient records, assisting with billing procedures, and delivering culturally competent care to diverse populations. The role appeals to candidates seeking a collaborative environment rooted in community support and professional growth. Opportunities for advancement are available within a fast-paced healthcare setting that values connection and positive change. The position requires travel to various locations and is based on-site.

The Associate Site Manager role within Johnson & Johnson Innovative Medicine serves as the primary liaison between the sponsor and clinical trial sites across the Central United States. Key responsibilities include ensuring site compliance with Good Clinical Practice and company protocols, conducting on-site and remote monitoring, managing site start-up and close-out activities, and overseeing data accuracy and adverse event reporting. This position offers the opportunity to contribute to life-saving medical advancements while working within a collaborative, inclusive culture that values employee diversity. The role is based remotely in Texas but requires up to 60% travel to support assigned sites, offering a dynamic environment for professionals dedicated to clinical research excellence.

The Sr. Loan Closer role at JMAC Lending supports the Closing department within a fully remote, wholesale and correspondent lending environment. Key responsibilities include reviewing loan documents for accuracy and regulatory compliance, managing funding conditions to ensure timely disbursement, and preparing closing disclosures for investor delivery. This position requires five years of mortgage experience and a strong grasp of TRID guidelines and various loan programs. The opportunity appeals to professionals seeking a culture built on integrity and continuous education, offering flexible Pacific Time hours, comprehensive health benefits, and a supportive team environment focused on ethical standards and operational excellence.