Jobs at Triad Technologies, LLC

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.

This full-time Senior Nurse Manager role leads the outpatient cardiology team at Emory Healthcare, focusing specifically on cardiac device patient care. The position requires a leader with prior cardiac device experience to oversee daily clinical operations, manage staff performance, and ensure compliance with safety and quality standards. Key responsibilities include driving clinical practice development, fostering a collaborative culture, and implementing evidence-based initiatives to enhance patient outcomes. The role offers a supportive environment with access to mentorship, leadership development programs, and comprehensive benefits. Working a standard Monday through Friday schedule, the position is ideal for a professional seeking to advance their career within a Magnet-designated academic health system.

The Emergency Department Assistant Nurse Manager role at Emory University Hospital Midtown supports the leadership team in overseeing daily clinical and operational functions during the 8pm to 6:30am shift. Key responsibilities include fostering a collaborative culture, managing staff performance and professional development, and ensuring compliance with safety and quality standards. This position offers the opportunity to work within a Magnet-certified academic health system that prioritizes staff well-being and continuous growth. The role provides access to comprehensive benefits, mentorship programs, and a supportive environment designed to help professionals reach new heights in their careers.

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.

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.

This full-time Clinical Trial Coordinator II role supports the planning and execution of global clinical studies within a fast-paced pharmaceutical environment. The position involves reviewing essential study documentation, overseeing risk-based monitoring, and ensuring regulatory inspection readiness in collaboration with study teams and external vendors. The role offers the opportunity to work on high-complexity Phase 2 and 3 trials across multiple therapeutic areas while developing expertise in international compliance standards. The position is based in an office setting with standard business hours, providing a collaborative atmosphere for professionals seeking to advance their careers in clinical research operations.

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.

The Clinical Trial Associate role at Crinetics supports the development of therapies for endocrine diseases within a patient-centric, team-oriented culture. Key responsibilities include executing study activities according to protocols, managing regulatory documents and Trial Master Files, and coordinating study start-up, conduct, and closeout phases. The position requires collaboration with cross-functional teams and external vendors to ensure high-quality outcomes and compliance with Good Clinical Practice guidelines. This opportunity appeals to candidates seeking to contribute to meaningful medical innovation in an inclusive, dog-friendly environment. The role is based in San Diego with minimal travel requirements of up to 5%.

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.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional teams to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the end-to-end management of human samples, including collection, processing, storage, and shipping, while ensuring strict compliance with study protocols and informed consent forms. The position also involves coordinating with data management leads for sample data acquisition, forecasting operational costs, and resolving sample-related queries with clinical sites and CROs. The role appeals to professionals seeking a remote opportunity within a collaborative environment that values scientific translation and operational excellence. It offers the chance to work independently on complex clinical trials while contributing to a mission-driven team focused on advancing medicine.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional teams to ensure high-quality sample and data delivery for clinical trials. Key responsibilities include overseeing the entire lifecycle of human sample management, from collection and processing to storage and shipping, while coordinating with data management leads to ensure accurate data capture and compliance with study protocols. The position also involves managing vendor relationships, forecasting operational costs, and providing technical guidance to clinical sites. The role offers the appeal of working within a collaborative environment that translates scientific research into medicine, with opportunities for professional growth in a remote setting.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional teams to ensure high-quality sample and data delivery for clinical trials. Key responsibilities include overseeing the end-to-end management of human samples, from collection and processing to storage and shipping, while ensuring strict protocol compliance. The position also involves coordinating with data management leads for sample data integration, forecasting operational costs, and providing technical guidance to clinical sites. The role offers the opportunity to work remotely within a collaborative environment that values scientific translation and professional growth. Candidates will leverage their clinical research background to drive operational excellence and support the company's mission of advancing medicine through biomarker evaluation.

This senior clinical research associate role at ICON plc focuses on ophthalmology trials within a global healthcare intelligence organization. The position involves overseeing clinical trial activities to ensure strict adherence to protocols, regulatory requirements, and Good Clinical Practice standards. Key responsibilities include conducting site visits to assess performance, resolving operational issues, collaborating with cross-functional teams for accurate data reporting, and providing mentorship to junior staff. The role appeals to professionals seeking a culture that values inclusion, innovation, and talent development. It offers a flexible benefits package focused on well-being and work-life balance, with a work arrangement requiring approximately 60% travel to manage multiple sites.

This senior clinical research associate role at ICON plc focuses on ophthalmology trials within a global healthcare intelligence organization. The position involves leading complex monitoring tasks to ensure sites adhere to protocols, regulatory standards, and Good Clinical Practice. Key responsibilities include conducting site visits to assess performance, collaborating with cross-functional teams for accurate data reporting, and providing mentorship to junior staff. The role appeals to professionals seeking a diverse, inclusive culture that rewards high performance and supports work-life balance through comprehensive benefits. While the position requires approximately 60% travel, it offers significant opportunities for professional growth and the chance to shape the future of clinical development.