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Technical Reporting Associate

Labcorp
0-1 years
INR 3.5 LPA – 5.5 LPA
Bangalore, India
1 June 24, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

TECHNICAL REPORTING ASSOCIATE I

Company: Labcorp
Location: Bangalore, Karnataka, India
Department: Global Reporting Solutions / Lab Operations
Job Type: Full-Time
Work Mode: On-Site

JOB OVERVIEW

Labcorp is seeking a Technical Reporting Associate I to support non-clinical studies and the preparation of scientific study reports. This entry-level role involves data table preparation, report generation, quality control activities, and the use of reporting software tools to ensure accurate and timely delivery of study-related documentation.

WORK SCHEDULE

  • Monday to Friday

  • 2:00 PM – 11:00 PM IST

KEY RESPONSIBILITIES

Data Table Preparation

  • Review study protocols and understand study designs.

  • Prepare data tables for study updates using reporting and table-generation software.

  • Perform basic statistical analyses and incorporate results into study reports.

  • Prepare CTD (Common Technical Document) tabulated summaries.

  • Draft and quality-check manually prepared data tables.

  • Input study data into Microsoft Excel and transfer outputs into Microsoft Word for report preparation.

  • Ensure accuracy and completeness of all study-related data tables.

  • Perform quality control (QC) activities on reports and data outputs.

Reporting & Documentation

  • Utilize reporting software tools including:

    • ToxReporting

    • Microsoft Excel

    • Microsoft Word

    • Database and collaboration tools

  • Support the production of non-clinical study reports.

  • Maintain reporting documentation according to internal quality standards.

  • Learn and execute additional reporting-related duties as assigned.

Project & Scheduling Responsibilities

  • Organize and prioritize assigned work to meet project timelines.

  • Manage multiple studies with varying designs and reporting requirements.

  • Communicate project progress and delivery challenges to supervisors and study teams.

  • Collaborate with Global Reporting Solutions and Study Direction teams.

  • Support training and mentoring of new team members after gaining experience.

  • Participate in peer review activities to ensure report quality.

EDUCATIONAL QUALIFICATIONS

Required

  • Bachelor’s Degree in Science

Preferred

  • Master’s Degree in Science

EXPERIENCE

  • Freshers and early-career candidates can apply.

  • Experience in scientific reporting, laboratory operations, toxicology reporting, or clinical research reporting is an advantage.

  • Knowledge of data handling and reporting tools preferred.