Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Technical Reporting Associate

Labcorp
0-1 years
INR 3.5 LPA – 5 LPA
Bangalore, India
1 June 26, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Technical Reporting Associate I

Company: Labcorp
Location: Bangalore, India
Department: Global Reporting Solutions – Lab Operations
Job Type: Full-Time
Work Schedule: Monday – Friday (2:00 PM – 11:00 PM)


JOB OVERVIEW

The Technical Reporting Associate I supports non-clinical study reporting by preparing, validating, and quality-checking scientific data tables and study reports. The role involves working with reporting software, Microsoft Office applications, statistical data, and technical documentation to ensure accurate, high-quality, and regulatory-compliant non-clinical study reports. This position is ideal for science graduates looking to build a career in laboratory reporting, toxicology reporting, and scientific documentation.


KEY RESPONSIBILITIES

Technical Reporting

  • Prepare technical reports for non-clinical studies.

  • Support the production of scientific study reports.

  • Create and maintain reporting documentation.

  • Ensure report accuracy and completeness.

  • Follow reporting SOPs and quality standards.

Data Table Preparation

  • Prepare study data tables using reporting software.

  • Generate statistical data tables for study updates.

  • Create CTD tabulated summaries.

  • Transfer study data from Excel to Word reports.

  • Review tables for accuracy and consistency.

Quality Control

  • Perform quality checks on reports and data tables.

  • Verify manually prepared data tables.

  • Identify and correct reporting errors.

  • Ensure data integrity and documentation quality.

  • Support internal QC activities.

Data Management

  • Understand study protocols and reporting requirements.

  • Manage reporting datasets using software tools.

  • Organize and maintain reporting files.

  • Handle multiple study assignments efficiently.

  • Maintain accurate documentation.

Team Collaboration

  • Coordinate with Study Direction and Reporting teams.

  • Communicate project status and delivery timelines.

  • Assist in mentoring new team members after training.

  • Participate in workflow improvements.

  • Support reporting-related activities as assigned.


EDUCATIONAL QUALIFICATIONS

Required

  • Bachelor's Degree in Science

Preferred

  • Master's Degree in Science


EXPERIENCE REQUIREMENTS

Required

  • Freshers and entry-level candidates are encouraged to apply.