We are currently seeking a Sr. Research Nurse to implement and oversee multiple, single-center and multi-site national studies as assigned for the division of Transplant Oncology and Infectious Disease (TOID). Our primary research is related to the use of novel organ sources to address the national organ shortage, such as HIV+ to HIV+ transplant under the HOPE Act. The Sr. Research Nurse should be someone who works well in a fast-paced collaborative atmosphere but can also maintain a high degree of independence. This position will report directly to the TOID Research Nurse Manager, Operational Manager, and Principal Investigator. DUTIES AND RESPONSIBILITIES Project Management Pre-study - Anticipates research requirements for designated patient populations. - Collaborates in development & writing of protocols and consent forms, as appropriate. - Collaborates in the development and preparation of regulatory documents as appropriate - Applies knowledge of study design to evaluate new protocols. - Applies knowledge of federal & local regulations when evaluating new protocols. - Reviews & assesses new protocols for clarity, thoroughness, logistical feasibility, maintaining subject safety, etc., for assigned protocols. - Collaborates in the determination of roles & responsibilities of research team members in the implementation of assigned trials. - Evaluates the impact on & availability of resources for assigned clinical trials. - Lists & clarifies concerns & questions about new protocols with Research Nurse Manager and PI. Proposes & negotiates alternatives to improve protocol implementation. Pre-initiation - Collaborates in the design of appropriate methods for the collection of data required for assigned trials. - Oversees & collaborates in development of study tools, including data collection forms, eligibility checklists, preprinted orders, & distribution of the protocol on the Web Library and Internet (where applicable). - Develops study-specific CRFs. - Participates in the development of study-specific databases, assuring clinical data is appropriate for answering study-specific endpoints. - Develops study-specific laboratory and operational manuals. - Oversees that regulatory requirements are met for designated studies. - Assures compliance with local, national, and international regulatory standards; as appropriate, prepares & submits required regulatory documents. - Develop training materials for assigned studies/projects. - Monitors for and notifies PI of IRB approval/request for further information as appropriate. - Determines that IRB approval has been received before initiation of research activity. - Represents the department at research and protocol initiation meetings. - Assures that all elements of a trial are in place before activating sites. - Participates in communications with protocol sponsors, NCI, and the cooperative group and coordinates plans to address issues with the PI. Recruitment & enrollment - Responsible for evaluating and assuring recruitment and study/project goals are met by the research team and participating sites. - Responsible for the development of recruitment strategies to ensure patient accrual within protocol timeframes. - Prepares and presents study-specific updates to Research Nurse Manager, Operations Manager, and Investigators as requested. Identify and provide recommendations to remediate issues of concern. Data Management/Document maintenance - Ensures collection of pertinent data from internal & external sources & monitors compliance with requirements of assigned clinical trials. - Applies clinical/pharmacological knowledge to ensure that safety reporting processes for assigned studies are implemented and maintained. - Prepares and submits protocol amendments and revisions as appropriate. - Demonstrates ability to manage multiple projects at different stages of the clinical research process. - Demonstrates ability to integrate new clinical trials with current research activity. Quality Assurance - Evaluates outcomes of clinical trials. - Monitors external sites' compliance with required study procedures & GCP standards. - Performs/monitors ongoing data analysis regarding clinical research studies, including toxicities, dose modifications, dose levels, adverse reactions, & response. - Assumes responsibility for specific QA activities for research teams (i.e., participates in institutional QA process). - Participates in sponsor/cooperative group/internal audits/monitoring. - Assists with development & review of TOID SOPs for the performance of clinical research. - Maintains records of correspondence of faxes, e-mails, IRB/JCCI submissions, FDA submissions, etc. Staff Education - Participates in the orientation process for new Clinical Research Nurses and Clinical Research Coordinators, including the mentoring and management of other clinic personnel to promote quality, safety, and excellence in care. - Coordinates and/or presents continuing education/in-service programs for Clinical Research Nurses, Clinical Associates, Data Managers, and others involved in the research process. - Attends and participates in in-service and external trainings, workshops, conferences, and other relevant programs for professional growth and development. Other - Collaborates with other members of the research team in preparing study results for presentation/publication. - Authors/coauthors manuscripts for publication in the nursing literature and/or presentation at conferences related to areas of expertise. - Identifies nursing research questions related to protocol populations/issues and, with assistance, collaboration, and appropriate financial support, implements nursing research within departmental priorities. - Takes advantage of opportunities to make presentations in the local community regarding research projects, areas of expertise, etc. Minimum Qualifications - Individual must be a registered nurse, licensed in the State of Maryland - Minimum of two years of experience in the specialty or a related area required. Classified Title: Sr. Research Nurse Role/Level/Range: ACRP/04/MF Starting Salary Range: $38.51 - $67.53 HRLY ($80,000 targeted; Commensurate w/exp.) Employee group: Casual / On Call Schedule: flexible FLSA Status: Exempt Location: Remote Department name: SOM DOM Infectious Disease Personnel area: School of Medicine

Overview Keysight is at the forefront of technology innovation, delivering breakthroughs and trusted insights in electronic design, simulation, prototyping, test, manufacturing, and optimization. Our ~15,000 employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over 100 countries. Learn more about what we do. Our award-winning culture embraces a bold vision of where technology can take us and a passion for tackling challenging problems with industry-first solutions. We believe that when people feel a sense of belonging, they can be more creative, innovative, and thrive at all points in their careers. Responsibilities Platform Administration & Lifecycle Management - Administer and enhance the Morpheus Enterprise Software platform to automate provisioning, scaling, and lifecycle management of virtual machines, Kubernetes clusters, and related infrastructure. - Manage underlying infrastructure hosts (e.g., vSphere, OLVM) and clusters - Maintain and enhance the Image Catalog to enable secure self-service provisioning for development teams. - Manage templates, blueprints, and automation workflows within Morpheus for consistent and compliant infrastructure delivery. Kubernetes and Container Platform Operations - Provision and manage Kubernetes clusters for containerized build pipelines and development/test environments in controlled networks. - Collaborate with DevOps engineers to enforce security baselines, air-gapped operations (where needed), and approved container sources. - Establish infrastructure guardrails ensuring compliance with supply chain security requirements. Infrastructure Automation & Integration - Develop and maintain Ansible playbooks, scripts, and automation pipelines to configure hosts, clusters, and platforms consistently across environments. - Work closely with Security and Compliance teams to ensure platform configurations align with NIST 800-218 (SSDF) and NIST 800-171. - Integrate platforms with secure CI/CD systems (e.g., CloudBees Jenkins), artifact management (JFrog Artifactory), and observability platforms (Splunk, Zabbix). Performance, Monitoring, and Reliability - Monitor platform health and performance; proactively resolve issues impacting secure builds, developers, or test teams. - Create and maintain dashboards, alerts, and performance metrics for platform services. - Lead efforts to improve platform resiliency, backup, and disaster recovery processes. Security & Compliance - Ensure platforms meet all applicable security and compliance controls, including: - Network segmentation and isolation. - Strong access controls and RBAC. - Secure audit logging and retention. - Vulnerability management, patching, and configuration management aligned with NIST. - Support internal and external audits, including providing evidence of compliance. Qualifications Required Qualifications - Bachelor’s or Master’s degree in Computer Science, Engineering, or equivalent experience. - 4+ years of experience in infrastructure or platform engineering. - Hands-on experience with platforms like Morpheus Data, CloudBolt, VMware vSphere, OLVM, or OpenShift. - Strong Linux system administration skills (RHEL/CentOS/Ubuntu) with automation expertise in Ansible. - Experience provisioning and managing Kubernetes clusters (Rancher, OpenShift, EKS, etc.). - Expertise in secure infrastructure management within controlled environments. - Experience integrating infrastructure platforms with CI/CD, observability, and security tools. Preferred Qualifications - Experience with Morpheus Enterprise Software or similar platforms. - Background in aerospace, defense, or government programs. - Familiarity with NIST 800-53, CMMC, and supply-chain security. - Experience with monitoring and secrets management platforms. - Solid knowledge of networking, storage, and virtualization in air-gapped or segmented environments. - Relevant certifications preferred: - Morpheus Data Certified Administrator. - Certified Kubernetes Administrator (CKA). - Red Hat Certified Engineer (RHCE). - ITIL, CISSP, or similar compliance/security certifications. Skills - Strong collaboration and communication skills to work across R&D, DevOps, IT, Security, and Compliance teams. - Ability to develop and document repeatable processes and operational runbooks. - Analytical thinker with a focus on automation and continuous improvement. Careers Privacy Statement***Keysight is an Equal Opportunity Employer.***

Per Diem Research Nurse - Independent Contractor - Sarnia, Ontario Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives. Job Responsibilities - Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs. - Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information. - Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements. - Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi- disciplinary, project management and client-facing meetings. - Coordinate (working with the RN team) and complete subject trial visits on- and off-site. Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately. - Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs. - Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents. - Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on- and off-site care. - Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required. - Report any suspected misconduct or fraud to Illingworth and associated companies. Qualifications: - Registered nurse with a minimum of 2 years' post qualification experience. - Experience on site/CRC experience - Extensive experience in Phlebotomy in patient facing scenarios - Research and clinical trials experience with GCP certification. - Knowledge of research design and methodology desirable. - Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable. - Ability to work autonomously with initiative in a team within a multidisciplinary environment. - Excellent verbal and written communication skills. - Ability to prioritize and manage multiple tasks. - Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum. Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Research Associate I Evidera– Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotech's, spanning 2,700 clinical trials across 100+ countries in the last 5 years. What You'll Do: - Assist with preparing proposals, protocols, and reports by conducting internet and literature searches. - Conduct literature reviews by abstracting data from scientific articles. - Participate in and oversee site recruitment, site contracting and IRB submissions, site management, and site training (including tracking enrollment and scheduling). - Manage data, including performing data entry and review. Assist with data analysis, including preparing qualitative code books, performing and overseeing coding, and reviewing quantitative data tables. Conduct one-on-one cognitive interviews and co-moderating focus groups; compile data collection tools. Handle data extraction (epidemiological and clinical data); model programming (larger parts of models). - Perform efficient delegation and communication within and outside of the project team. - Assist with financial management. - Provide scientific support in the implementation of simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., Markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. - Assist project managers on multiple projects including drafting sections of project deliverables (reports, dossiers, protocols, spreadsheets, etc.) and participate in abstract, manuscript preparation, project proposals (e.g., gathering relevant material, drafting background sections, conducting scoping searches, and developing project budgets). - Participate in client meetings and prepare meeting minutes. Education and Experience Requirements: - Master’s Degree in scientific discipline and at least one year of experience in healthcare research; or bachelor’s degree in scientific discipline and at least two years of experience in healthcare research. - Coursework in implementation science and/or experience with implementation science studies In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities: - Good knowledge of Microsoft Office - Basic understanding of research methods - Basic knowledge of implementation science theories, models, and frameworks and/or behavioral theories, models and frameworks - Know how to multitask - Good communication skills - Problem-solving mindset - Attention to detail - Ability to work well within a team Working Environment: Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: • Travel 10–30% of the time Why join us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs. Compensation and Benefits The salary range estimated for this position based in District of Columbia is $80,000.00–$90,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: - A choice of national medical and dental plans, and a national vision plan, including health incentive programs - Employee assistance and family support programs, including commuter benefits and tuition reimbursement - At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy - Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan - Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards