15 Crio Jobs

Role Overview: As a Senior Manager - Cloud Subject Matter Expert (SME) specializing in Red Hat OpenShift, you will play a crucial role in designing, implementing, and managing a consolidated platform built on Red Hat OpenShift Container Platform (RHOCP). Your expertise in running containerized workloads and traditional Virtual Machines (VMs) using OpenShift Virtualization will be essential in ensuring the performance, reliability, and cost efficiency of the hybrid environment. You will manage and operate Telco Cloud platforms on Red Hat OpenShift and Private Cloud Virtualization environments to support VNF/CNF workloads. Key Responsibilities: - Manage daily operations of Red Hat OpenShift an...

Position Overview We are seeking an experienced Clinical Data Specialist II to join our clinical research team in Chennai. The successful candidate will be responsible for accurate and timely data entry into Electronic Data Capture (EDC) systems from various e-source documents, including real-time data and Clinical Research Information Officer (CRIO) sources. Key Responsibilities Data Management Perform accurate data entry into EDC systems from e-source documents (Real-time & CRIO). Conduct data verification and validation to ensure data integrity. Execute data reconciliation activities between different data sources & EDC. Maintain detailed logs of data entry activities and progress trackin...

We are hiring for Labview Designer experience-6-8yrs Location- Pune jd- 6 - 10 years working with the following technologies: o LabVIEW 2017 or above. o working experience with different protocols (TCP/IP, Network streams, EithernetIP etc). o Strong Experience implementing solutions involving cRIO and FPGA. o Strong Experience implementing solutions involving PXIe. Good Communication Skills (Verbal + Written) Proficient troubleshooting skills Certification in mentioned skills

Role : Regulatory Specialist Location : Chennai, Tamil Nadu Experience : 7+ Years Job Requirements: Bachelor's degree in Life Sciences, Clinical Research, Science, Healthcare Administration, or a related field. 25 years of regulatory experience in clinical research or pharmaceutical environments. CITI certifications (GCP, HSC, RCR, COI, IPS, IATA, ICH, CRC) required within two weeks of hire; training will be provided. Familiarity with IRB submissions, study start-up activities, and regulatory document maintenance. Proficiency with CRIO (Clinical Research IO) or similar electronic platforms used for eISF and study documentation. Experience with Clinical Trial Management Systems (CTMS), Electr...

Role : Clinical Research Project Manager Location : Chennai, Tamil Nadu Experience : 10-15 Years Requirements: 1012 years of direct, hands-on experience in clinical trials, with a focus on interventional studies (Phase IIV). Proven ability to read, interpret, and operationalize clinical trial protocols into eSource/EDC workflows. Experience managing end-to-end clinical trial processes including start-up, site initiation, data collection, query management, and close-out. Minimum 45 years of people management experience with demonstrated success mentoring and leading CDM/clinical trial teams. Strong expertise in clinical trial systems CTMS (CRIO preferred), eSource, and EDC platforms. Backgrou...

Your role and responsibilities Designs and provisions RedHat OpenShift infrastructure considering Cloud native architecture and deployment models. Creates RedHat Container Platform Cluster. Implements OpenShift PaaS DevOps Toolchain. Experienced in OpenShift Component services in Compute, Storage, Networking and monitoring of applications. Deploys and implements Ansible playbooks. Implements task control, deploying files to manage host and host pattern design, role and policy based playbook creation, optimize compute, storage and network service design. Holds the certification associated with this skillRed Hat Certified Specialist in OpenShift Administration. Performs Infrastructure as code ...

As a Clinical Data Coordinator at our company, your role will involve managing clinical data efficiently to support research activities. Your key responsibilities will include: - Conducting clinical data management tasks - Utilizing CRIO software for data organization - Working with eSource systems for data collection - Supporting clinical research activities To excel in this role, you should have the following qualifications: - 2-5 years of experience in clinical data management - Proficiency in CRIO software - Familiarity with eSource systems - Background in clinical research If you are passionate about contributing to cutting-edge research and have a strong foundation in clinical data man...

Role Overview: As a Senior LabView Developer at BBS-Automation in Pune, your main responsibility will be to develop LabView applications, integrate software and hardware components, and troubleshoot system issues. You will also be involved in designing and implementing test solutions while providing technical support to the team. Key Responsibilities: - Design, develop, and maintain LabVIEW-based applications for test, measurement, and automation systems. - Interface and integrate hardware such as DAQs, PXI, cRIO, GPIB, serial devices, and sensors. - Develop TestStand sequences and integrate them with LabVIEW for automated test execution (if applicable). - Conduct system debugging, troublesh...

Responsible for managing the CRIO platform, creating eSource templates, and supporting study teams with system setup, training, and compliance to ensure efficient, high-quality clinical trial execution.

Job Summary: We are looking for a skilled LabVIEW Developer with experience in camera-based vision systems to join our engineering team. You will design and develop custom software solutions for test automation, data acquisition, and machine vision inspection using NI LabVIEW and the NI Vision Development Module (VDM). The ideal candidate has hands-on experience integrating cameras, performing image processing, and developing automated visual inspection systems in industrial or R&D settings. Key Responsibilities: • Design, develop, and deploy LabVIEW applications for automated test, measurement, and vision-based inspection systems. Integrate and configure industrial cameras (USB, GigE, FireW...

Role : Senior Clinical Data Manager Location : Chennai, Tamil Nadu Experience : 10-15 Years Requirements: 10-15 years of experience in clinical trial/data management and data operations. Minimum 4-5 years of people management (preferred) experience with proven supervisory skills. Extensive experience with CTMS platforms (CRIO, RT CTMS, Veeva Vault CTMS, or similar). Strong background in EDC systems management and clinical data operations. Experience in pharmaceutical, biotechnology, or CRO environment across multiple therapeutic areas. Technical Expertise: CTMS configuration and administration skills (Having knowledge in CRIO is an advantage). Deep knowledge of EDC platforms and system integ...

Role Overview: As a liaison between Development teams and Platform (PAAS) teams, you will be responsible for translating requirements into technical tasks or support requests. You will use coding languages or scripting methodologies to solve problems with custom workflows. Your role involves documenting problems, articulating solutions or workarounds, and being a key contributor on projects to brainstorm the best way to tackle complex technological infrastructure, security, or development problems. Key Responsibilities: - Translate requirements into technical tasks or support requests - Use coding languages or scripting methodologies to solve problems with custom workflows - Document problem...

Knowledge of kubernetes concepts like pods, services, deployments, statefulsets. Candidate must have Operational experience in Kubernetes K8 installing, managing, and upgrading Kubernetes cluster (DC On-Prem) environment. Must have experience on Docker, Podman, containerd and CRIO CRI. Familiarity with Kubernetes networking, including CNI plugins, ingress controllers and service meshes. Must have knowledge on K8S deployment and good to have helm chart knowledge. Implement security measures and ensure compliance with security policies and procedures like CIS benchmark. Understanding of Kubernetes security best practices, like RBAC, network, and pod security policies. Collaborate with other te...

Position Overview We are seeking an experienced Clinical Data Specialist II to join our clinical research team in Chennai. The successful candidate will be responsible for accurate and timely data entry into Electronic Data Capture (EDC) systems from various e-source documents, including real-time data and Clinical Research Information Officer (CRIO) sources. Key Responsibilities Data Management Perform accurate data entry into EDC systems from e-source documents (Real-time & CRIO). Conduct data verification and validation to ensure data integrity. Execute data reconciliation activities between different data sources & EDC. Maintain detailed logs of data entry activities and progress trackin...

As a Technical Implementation Engineer, you will play a crucial role in the onboarding process of customers to various Qualys products, with a primary focus on Enterprise TruRisk Management (ETM). Your responsibilities will revolve around acting as a trusted advisor to customers, guiding them through the integration of Qualys solutions into their environments, aligning these implementations with their security objectives, and ensuring their success with the platform. This position emphasizes expertise in DevOps, cloud security, and enabling customers to fully leverage Qualys solutions to achieve their security goals. Your key responsibilities will include managing the onboarding process for ...