Navitas

Navitas Life Sciences is a technology-backed global clinical research organization, headquartered in Princeton, NJ, with over 1000 employees and spread across 5 countries.

At Navitas Life Sciences, we are committed to accelerate time to market for life-saving therapies. We are a technology-driven CRO with end-to-end and point services and solutions for drug development and beyond. We provide outsourced data science, regulatory & safety, and full-service CRO services to large and mid-sized biopharmaceutical clients. Navitas Clinical Research provides full service CRO offerings to global biopharma companies. Navitas Data Sciences is our global clinical data functional service provider.

Job Title:

Software Trainee

Last Date To Apply:

Not Specified

(Apply Link at the end)

ASAP, will end as soon as a certain number is reached

Experience Level:

Candidate Should have 0-1 year of experience

Job Location:

Chennai,  India

Salary:

Not Specified

Eligible Batches:

Not Specified

Requirements:

• 0-1 years’ experience
• Knowledge in OOP concepts and design principles
• Excellent verbal communication
• Good team player
• Awareness of latest computer technology

Job Description:

• Monitoring DocFlow for upcoming reports and assigning as appropriate to an Aggregate Data Management Specialist.
• Refreshing preliminary tables at DLP-45 and sends to the client PSSR authors
• Receiving requests for tables from client
• Communicating with the requestor to get clarity on Table Requests
• Answering questions on table generated from requestor
• Generating all the requested data tables
• Quality control and peer QC of data table
• Uploading tables into GDMS
• Informing PSSR Authors that the data tables are available in GDMS
• Creating aggregate case lists after the report was submitted to the agencies
• Learning and maintaining a working knowledge of data table generation systems and tools and how these are applied
• On-going liaison with PSSR Authors to ensure data table standards and deadlines for delivery are met
• Recording of key information (including workflow) to support delivery of metrics
• Adhering to the appropriate use of technical tools, through use of working practices and QC/QA regimes, such that regulatory and internal compliance is preserved