Spotfire Programmer : Life Science : Apply Now Outpace Consulting Services

3 - 8 years

6 - 15 Lacs

Ahmedabad, Bengaluru

Work from Office

Hi, We are hiring for ITES Company for Spotfire Programmer Role. Job description: Minimum 3 years of experience as a Spotfire Programmer and Clinical experience is Mandatory Working on Refreshes requests for SRT & CSTV Building Oncology & Standard Visuals for Clinical Study Team Visualization (CSTV) Setting up standard and Study Specific Spotfire requests for Safety Review Team (SRT) Knowledge of Spotfire, Study configuration tool and On Demand Tool. Creating SAS Codes as per the requirement Setup and customization of visuals for Medical Reviewers Validation of visuals as per the specifications Optimize data models and queries for improved performance and scalability. Monitor and troubleshoot issues related to the Spotfire platform and coordinate with vendors for advanced support. Seeking opportunities to leverage expertise in Spotfire development and data visualization to contribute to the success of a data-driven organization. Integrate and prepare data, create visualizations and reports, optimize performance, and collaborate with stakeholders. Possesses a strong understanding of data exploration, ETL processes, and programming in R. Adept at collaborating with clients and stakeholders to translate complex data into clear and actionable insights. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Bangalore Search : Spotfire Programmer Bangalore (Job Code # 80) b) For Position in Ahmedabad Search : Spotfire Programmer Ahmedabad (Job Code # 82)

Posted 3 months ago

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Medical Intelligence & Analytics Lead Careernet

4.0 - 9.0 years

7 - 15 Lacs

bengaluru

Hybrid

Key Skills: Clinical Programming, Clinical Data Management, UAT Roles and Responsibilities: Lead and manage clinical data programming and data management activities across multiple trials. Oversee and execute User Acceptance Testing (UAT) to validate system functionalities and ensure data quality. Handle end-to-end data activities including eCRF development, database lock/unlock, and clinical coding. Ensure accurate and timely SAE reconciliation in accordance with regulatory standards. Collaborate with clinical operations, biostatistics, and medical affairs to support smooth trial conduct. Utilize EDC platforms like Medidata Rave, Oracle Inform, and Veeva for efficient data collection and study tracking. Ensure all data processes are compliant with industry regulations and standard operating procedures. Continuously improve data workflows and contribute to knowledge sharing within the team. Skills Required: Must-Have: Strong experience in Clinical Programming and Clinical Data Management Proficiency in conducting User Acceptance Testing (UAT) Solid understanding of clinical trial data lifecycle and regulatory requirements Hands-on expertise with eCRF processes, clinical coding, and SAE reconciliation Nice-to-Have: Working knowledge of EDC systems such as Rave, Inform, and Veeva Familiarity with healthcare analytics tools and data visualization platforms Understanding of medical terminology and clinical trial documentation Education: Graduate in Computer Applications or a related field.

Posted Date not available

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Senior Analyst - Clinical Data Management Careernet

4.0 - 6.0 years

10 - 16 Lacs

bengaluru

Hybrid

Key Skills: Clinical Programming, Clinical Data Management, Veeam, Imaging, Medical Imaging Roles and Responsibilities: Act as the Trial Data Manager for 3-4 studies simultaneously, while overseeing data management for additional trials. Provide leadership in defining and executing data management plans across the study lifecycle. Review clinical protocols and offer feedback to enhance clarity and optimize data collection design. Lead the planning and execution of eCRF design, database development, and UAT processes. Manage and validate external data according to protocol requirements and predefined standards. Ensure timely and accurate data cleaning, query resolution, and database lock activities. Monitor trial progress and milestones; provide status updates and risk assessments to stakeholders. Collaborate closely with the Clinical Trial Team (CTT) and Program Clinical Data Manager (PCDM). Enforce data standards including CDISC/CDASH and ensure regulatory compliance across trials. Mentor and support junior team members by sharing knowledge and promoting best practices. Maintain compliance with GCP, SOPs, and applicable regulatory guidelines. Stay informed about emerging tools, technologies, and industry data standards. Skills Required: Must-Have : Strong experience in Clinical Data Management and Clinical Programming Ability to manage multiple studies independently, ensuring quality and regulatory compliance Solid understanding of clinical trial processes, GCP, and data standards (e.g., CDISC) Experience with eCRF design, EDC systems, and data validation workflows Nice-to-Have: Familiarity with Medical Imaging or Imaging data within clinical trials Exposure to Veeam or similar imaging data management platforms Experience mentoring or managing junior data management professionals Knowledge of SAS, R, or other clinical programming tools is a plus Education: Bachelor's degree in Life Sciences, Computer Science, or a related field.

Posted Date not available

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