We are looking for a Software Dev Engr who will: - Code Development: Write, debug, and maintain high-quality code that meets project requirements. - Collaboration: Work closely with senior developers, designers, and product managers to understand requirements and deliver solutions. - Testing: Participate in unit testing, integration testing, and debugging of applications to ensure performance and scalability. - Documentation: Create and maintain technical documentation for codebases, APIs, and development processes. - Learning & Growth: Continuously enhance technical skills and stay updated with emerging technologies and industry best practices. - Code Review: Contribute to peer code reviews to ensure code quality and adherence to standards. - You should be able to collaborate effectively with other team members. - You will work independently in a cross-cultural environment, having 2-3 hours overlap with stakeholders in the US. Is this opportunity right for you? We are looking for candidates who: - Bachelor’s degree in computer science, or technically related field, or equivalent professional experience. - 3-5 years of experience in software development and software support/maintenance. - Experience in C#, .NET, MS SQL Server, Web Services, SOAP, and ASP.Net Core. - Experience in Cloud such as AWS. - Strong Knowledge of OOP concepts. - Work well within a team environment using Agile methods. - Familiarity with version control systems (Git) and CI/CD processes. - Collaborate with stakeholders to gather requirements. - Participate in code reviews and mentoring junior developers. - Strong proficiency in relevant programming languages and frameworks Soft Skills: - Strong problem-solving and analytical skills. - Eagerness to learn and adapt to new technologies. - Attention to detail and commitment to producing high-quality work. - Effective communication and teamwork skills. Location(s): India Remote Accommodation: If you would like to be considered for employment opportunities with CSG and need special assistance due to a disability or accommodation for a disability throughout any aspect of the application process, please call us at +1 (402) 431-7440 or email us at accommodations@csgi.com. CSG provides accommodations for persons with disabilities in employment, including during the hiring process and any interview and/or testing processes. Our Guiding Principles: Impact: Always help and empower others, whether they’re colleagues or customers. When our employees set their minds to something, great things happen. Integrity: Do what’s right for our customers and our people while being authentic. We treat everyone with trust and respect—that’s just who we are. Inspiration: Be bold in the way you think and passionate about the work you do. Test out innovative ideas without the fear of failure. Our Story: CSG empowers companies to build unforgettable experiences, making it easier for people and businesses to connect with, use and pay for the services they value most. For over 40 years, CSG's technologies and people have helped some of the world's most recognizable brands solve their toughest business challenges and evolve to meet the demands of today's digital economy. By channeling the power of all, we make ordinary customer and employee experiences extraordinary. Our people [CSGers] are fearlessly committed and connected, high on integrity and low on ego, making us the easiest company to do business with and the best place to work. We power a culture of integrity, innovation, and impact across our locations, representing the most authentic version of ourselves to build a better future together. That's just who we are. Learn more about CSG Inclusion & Impact here.

Software Engineer– Nike Inc.- Beaverton, OR. Apply big data technologies, develop, configure, and test programs, systems and solutions in order to meet defined digital product specifications and direction; design the backend architecture for data ingestion using tools like HBase, Spark Streaming/SQL, Elasticsearch on Amazon AWS for the system to capture data in real-time, batch updates with high read and write throughput; develop Terraform scripts as Infrastructure-As-A-Service using Amazon AWS Cloud services to deploy the backend infrastructure which includes Networks, Datastores, Compute Nodes, Code repos and Metric dashboards; assess a well-defined problem and lead the development of a technical solution that meets the needs of the business and aligns with architectural standards; manage small- to moderate-sized solutions; play a key role on larger teams, working within the parameters of two to three sprints; advise product owners on discrete technology-related business problems; formulate options, including assessing their relative merits and risks; work with product owners to determine the best solution; design and implement new features and fix defects in existing code base; write automated unit tests to validate code changes, write automated integration tests, and manually test changes in an integrated environment; and debug issues found during testing and troubleshoot issues in production environment. Telecommuting is available from anywhere in the U.S., except from AK, AL, AR, DE, HI, IA, ID, IN, KS, KY, LA, MT, ND, NE, NH, NM, NV, OH, OK, RI, SD, VT, WV, and WY. Must have a Master’s degree in Computer and Information Science, Engineering and 2 years of experience in the job offered or a engineering-related occupation. Position requires: • Powerbuilder • Git/Github • JavaScript • ServiceNow • JS Testing Framework such as Jest & Vitest • Webpack/Vite • Key AWS Infrastructure experience in Lambda, SNS, SQS, API Gateway • Dynamo DB • OpenSearch • DataBricks • Jenkins • Automation Anywhere (BOT Tool) • Shell Scripting • Dynatrace Apply at www.Nike.com/Careers (Job# R-82026) #LI-DNI We offer a number of accommodations to complete our interview process including screen readers, sign language interpreters, accessible and single location for in-person interviews, closed captioning, and other reasonable modifications as needed. If you discover, as you navigate our application process, that you need assistance or an accommodation due to a disability, please complete the Candidate Accommodation Request Form.

Principal Software Engineer – Nike Inc.- Beaverton, OR. Create and manage roadmaps with product and engineering leadership; Provide guidance on approaches to the implementation and realization of roadmaps; Collaborate with multiple multi-functional engineering teams within the company to build future product; Drive cross-domain alignment and technical delivery of major capabilities across value streams; Assess solution options based on their relative merits and risks to determine the best solution; Provide technical leadership in the evaluation, conceptualization, design, and development of major new capabilities; Assist in the establishment of core platforms and build a capability maturity vision to progress and improve our platforms; Architect and develop sophisticated solutions for testing and deployment; and Mentor software developers on the team through code reviews while ensuring that all work meets industry standards. Telecommuting is available from anywhere in the U.S., except from AK, AL, AR, DE, HI, IA, ID, IN, KS, KY, LA, MT, ND, NE, NH, NM, NV, OH, OK, RI, SD, VT, WV, and WY. Must have a Master’s degree in Computer Science, Mechanical Engineering, or Computer Information Systems and 2 years of experience in the job offered or in a computer-related occupation. Experience must include: • AWS • Java • Javascript • SEO • SQL • CI/CD • Azure • CDN and WAF • Splunk Apply at www.Nike.com/Careers (Job# R-81956) #LI-DNI We offer a number of accommodations to complete our interview process including screen readers, sign language interpreters, accessible and single location for in-person interviews, closed captioning, and other reasonable modifications as needed. If you discover, as you navigate our application process, that you need assistance or an accommodation due to a disability, please complete the Candidate Accommodation Request Form.

CRA II Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities - Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. - Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. - Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements - May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned. - Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. - Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. - Understands project scope, budgets, and timelines for own and others’ activities in the clinical team; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing priorities to achieve goals / targets. - May act as primary liaison with project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. - Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. - Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions. - May provide training or mentorship to more junior level CRAs. May perform training and sign off visits for junior CRA staff, as assigned. - May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL), or operational line manager. For Real World Late Phase (RWLP), the Sr. CRA I will use the business card title of Sr. Site Management Associate I. Additional responsibilities include:Site support throughout the study lifecycle from site identification through close out Knowledge of local requirements for real world late phase study designs Chart abstraction activities and data collection As required, collaborate and build relationships with Sponsor and other affiliates, medical science liaisons and local country staff Identify and communicate out of scope activities to Lead CRA/Project Manager Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associations Identify operational efficiencies and process improvements Develop country level informed consent forms Collaborate with RWLP Regulatory team to ensure updated regulatory information is applied and shared Participate in bid defense meetings Qualifications: - Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience - Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements - Must demonstrate good computer skills and be able to embrace new technologies - Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected. - Ability to manage required travel of up to 75% on a regular basis Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com 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.