Labcorp, a global leader in life sciences and clinical research services, is inviting applications for the position of Technical Reporting Associate I at its Bangalore, India location. This is an excellent opportunity for life science and pharmacy graduates seeking entry-level to early-career roles in technical reporting, regulatory documentation, and clinical data table preparation.
The role focuses on learning and executing end-to-end technical reporting activities, including CTD tabulated summaries, data table preparation, quality control (QC), and study documentation, supporting global nonclinical and toxicology studies.
Key Responsibilities – Technical Reporting Associate I
General Duties
- Learn and use reporting software tools including MS Word, Excel, table generation tools, databases, and collaboration platforms
- Manage a full study workload after completing role-specific training
- Provide basic mentoring and peer review support to junior team members post-training
- Ensure compliance with internal SOPs and reporting standards
Data Table Preparation & Reporting
- Understand study protocols and apply study design knowledge to prepare accurate data tables
- Perform basic statistical analysis using table generation software (e.g., ToxReporting)
- Review and QC data tables for accuracy and consistency
- Prepare CTD tabulated summaries aligned with study reports
- Manually input study data into MS Excel and integrate outputs into MS Word reports
- Perform routine and ad-hoc quality control (QC) checks
Scheduling & Coordination
- Plan and organize assigned work to meet project timelines
- Communicate proactively with supervisors, Global Reporting Solutions, and Study Direction teams
- Identify and escalate delivery risks or challenges in a timely manner
Eligibility & Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Toxicology, or related disciplines
- Freshers or candidates with 0–2 years of experience in clinical/nonclinical reporting, CROs, or regulatory documentation
- Strong attention to detail and data accuracy
- Basic knowledge of clinical or nonclinical study designs preferred
- Proficiency in MS Excel and MS Word
- Willingness to learn regulated documentation and reporting workflows
Why Join Labcorp?
- Work with a global CRO leader in regulated scientific reporting
- Structured training and career development in technical and regulatory reporting
- Exposure to CTD, toxicology, and nonclinical study documentation
- Inclusive and diverse workplace culture
- Competitive salary and benefits aligned with industry standards
Job Location
Bangalore, Karnataka, India
Employment Type
Full-Time | Permanent
Salary (Expected)
💰 ₹3.5 – ₹6.0 LPA (Indicative, based on skills and experience)
Application Deadline
⏰ Apply before: 23 December 2025
How to Apply
