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 troubleshoo...

Posted 7 months ago

AI Match Score

Apply

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 st...

Posted Date not available

AI Match Score

Apply

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 acti...

Posted Date not available

AI Match Score

Apply

Page 4 of 4

Previous 1 2 3 4

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.