Labcorp Hiring Technical Reporting Associate I - Bangalore
Are you seeking entry-level Labcorp Careers in India or Technical Reporting Associate Jobs in Bangalore? Leading diagnostics and drug development services provider Labcorp has announced recruitment for a **Technical Reporting Associate I** within its Global Reporting Solutions team based at its Bangalore office. This full-time, on-site position is open to freshers and recent science/pharmacy graduates.
The selected candidate will support non-clinical study reporting, compile study data tables, draft CTD summaries, and perform quality checks on reports. To prepare your application details, check out our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Technical Reporting Associate I |
| Company | Labcorp |
| Location | Bangalore, Karnataka, India (On-Site, Yeshwanthpur) |
| Work Mode | On-Site (Yeshwanthpur Facility) |
| Shift Timing | 2:00 PM – 11:00 PM IST (Monday to Friday) |
| Experience Required | Freshers & Entry-Level |
| Qualifications | B.Sc / M.Sc Science, B.Pharm, M.Pharm, or related Pharmaceutical/Biological Sciences |
| Department | Global Reporting Solutions / Lab Operations |
| Job ID | 2618325 |
| Salary Range | ₹4.5 LPA – ₹7.0 LPA (Approx.) |
| Application Deadline | Apply Immediately (Not Mentioned) |
💼 Key Responsibilities
1. Scientific Reporting Activities
- Support the preparation of non-clinical study reports for drug development programs.
- Assist in formatting and generating research reports for client deliverables.
- Utilize scientific documentation software and internal reporting applications.
2. Data Table Preparation
- Review and interpret study protocols and experimental designs.
- Compile study data tables and prepare statistical summaries using reporting platforms.
- Draft and perform quality checks on manually prepared data tables.
- Prepare Common Technical Document (CTD) tabulated summaries for regulatory filings.
- Transfer study data between reporting platforms when required, using MS Excel and MS Word.
3. Quality Control (QC) Activities
- Perform systematic quality checks on scientific reports to verify data accuracy.
- Review report outputs and formatting to ensure consistency and compliance with standards.
- Support quality assurance activities within study reporting workflows.
4. Documentation & Team Collaboration
- Maintain accurate study records and documentation logs to remain audit-ready.
- Coordinate with global reporting teams and study directors regarding deadlines.
- Escalate reporting issues and communicate project updates to managers.
Verifying clinical data and quality-checking data tables are closely related to database review. To learn more about clinical data and programming career pathways, read our detailed comparison on Clinical SAS vs Clinical Data Management.
🎓 Qualifications & Eligibility Criteria
Candidates applying for this entry-level reporting associate role should meet the following:
- Education: Bachelor’s Degree in Science (B.Sc) or equivalent required; a Master's Degree in Science (M.Sc) is preferred.
- Relevant Courses: B.Sc/M.Sc in Life Sciences, Biotechnology, Microbiology, Biochemistry, Chemistry, Biomedical Sciences, Zoology, B.Pharm, M.Pharm, Pharmaceutical Sciences, Clinical Research, Toxicology, or biological/pharmaceutical disciplines.
- Experience: Freshers and entry-level candidates are eligible to apply.
For pharmacy graduates planning their long-term path and comparing global career growth, check our salary and career guide on B.Pharm Career after Graduation: India vs USA.
Required Core Skills
- Exceptional attention to detail with data validation capabilities.
- Excellent written and verbal communication skills in English.
- Proficiency in Microsoft Office, particularly MS Excel and Word.
- Strong organizational, multitasking, and problem-solving skills.
- Ability to work independently as well as collaborate with global teams.
💰 Salary & Employee Benefits
- Expected Salary Package: ₹4.5 LPA – ₹7.0 LPA (CTC based on industry benchmarks).
- Direct entry into a globally recognized diagnostics and drug development services leader.
- Hands-on exposure to global scientific writing, ToxReporting software, and CTD summaries.
- Structured professional training and clear long-term career growth.
- On-site role featuring a stable work schedule (Monday to Friday, 2:00 PM – 11:00 PM IST).
Understanding study designs and lab testing guidelines is critical for clinical monitoring. Test your regulatory knowledge with our interactive Clinical Trial Assistant (CTA) Quiz.
🌟 Why Join Labcorp?
- Labcorp is a global diagnostic testing and drug development leader assisting organizations in developing innovative therapies.
- The Global Reporting Solutions team provides structured learning resources in documentation, QC, and database management.
- Highly collaborative environment offering exposure to international pharmaceutical projects.
📑 Resume Tips for Labcorp
- Highlight your academic degrees (B.Sc / M.Sc / B.Pharm / M.Pharm) and mention any projects related to data analysis or scientific reporting.
- Emphasize your proficiency in MS Excel and detail-oriented data validation skills.
- Keep your resume clean, structured, and optimized for Applicant Tracking Systems (ATS).
🎯 Labcorp Technical Reporting Associate Interview Questions
- What is a Common Technical Document (CTD), and why are tabulated summaries important?
- How do you ensure data accuracy when reviewing a 50-page data table?
- What MS Excel functions (e.g. VLOOKUP, pivot tables) are you familiar with for data organization?
- Describe your post-graduate project or a laboratory report you compiled.
- How do you manage your tasks and maintain quality when working in an evening shift (2:00 PM - 11:00 PM)?
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Labcorp's official job portal using the link below. Since no specific application deadline is mentioned, candidates are advised to apply immediately. For step-by-step guidance on setting up your profile, check out our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
No deadline is mentioned in the official post. Candidates are advised to apply immediately.
Q. Who is eligible to apply?
Candidates holding B.Sc, M.Sc, B.Pharm, M.Pharm in Science, Life Sciences, Biotechnology, Microbiology, Chemistry, or related fields.
Q. What are the shift timings?
The working hours are 2:00 PM to 11:00 PM IST, Monday to Friday.
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