Labcorp is hiring for the position of Data Associate I at its Yeshwantpur location in Bengaluru, Karnataka. This is a full-time opportunity with a rotating shift schedule.
The role involves supporting clinical and toxicology study data activities, including data entry, basic quality checks, data table preparation, protocol compliance review and assay validation workflows. The position also includes exposure to digital image data processing, slide scans and metadata management.
Candidates with a Bachelor’s degree in Science can apply. A Master’s degree in Science and approximately 6 months of clinical research industry experience are listed as preferred qualifications.
The application deadline for this vacancy is October 9, 2026.
Labcorp Data Associate I – Job Highlights
| Particular | Details |
|---|---|
| Company | Labcorp |
| Job Title | Data Associate I |
| Location | Yeshwantpur, Bengaluru, Karnataka |
| Job Type | Full Time |
| Work Schedule | Rotating Shift |
| Minimum Qualification | Bachelor’s Degree in Science |
| Preferred Qualification | Master’s Degree in Science |
| Preferred Experience | 6 Months in Clinical Research Industry |
| Key Areas | Clinical Data, Toxicology Data, Quality Checks, Data Processing |
| Requisition ID | 2635233 |
| Application Deadline | October 9, 2026 |
| Salary / CTC | Not specified |
About Labcorp
Labcorp is a global healthcare and laboratory services organization that provides scientific, diagnostic, data and technology solutions across healthcare and research.
The company works with healthcare providers, patients, researchers, pharmaceutical organizations and health systems. Its operations include laboratory services, clinical research and data-driven healthcare solutions.
Job Description
The Data Associate I will support data-related activities associated with clinical and toxicology studies. The role involves learning study protocols, entering and reviewing study data, preparing basic data tables and performing quality checks.
The position also provides exposure to assay validation workflows and digital image data processing, including slide scans and associated metadata.
The selected candidate will work under regular supervision and collaborate with cross-functional and global teams.
Data Associate I – Role Overview
The role is suitable for candidates with a scientific academic background who want to build experience in clinical research and data operations.
Key areas of work include:
- Study protocol understanding
- Toxicology study data entry
- Data quality checks
- Data table preparation
- Protocol compliance review
- Assay validation support
- Digital image data processing
- Metadata management
- Cross-functional collaboration
Educational Qualification
Minimum Qualification
Candidates must have a:
Bachelor’s Degree in Science
Preferred Qualification
A Master’s Degree in Science is preferred.
Experience Requirements
The vacancy lists 6 months of experience in the clinical research industry as a preferred qualification.
However, the minimum qualification specifically states a Bachelor’s degree in Science. Candidates should therefore review the official vacancy requirements carefully before applying.
Key Responsibilities
Study Protocol Understanding
The selected candidate will:
- Learn and develop proficiency in interpreting study protocols.
- Understand study requirements and applicable amendments.
- Apply protocol-related instructions while performing assigned data activities.
- Develop knowledge of regulatory and study-specific data requirements.
Toxicology Study Data Processing
Responsibilities include:
- Supporting back entry of toxicology study data.
- Entering information into the applicable data acquisition or collection database.
- Performing basic quality checks on entered data.
- Reviewing information for accuracy and completeness.
Data Tables and Quality Checks
The Data Associate I will learn to:
- Prepare data tables from manually collected study data.
- Verify the accuracy of prepared tables.
- Review data within the acquisition or collection database.
- Identify information that may not comply with protocol requirements.
- Support data quality activities.
Protocol and Regulatory Compliance
The role includes reviewing study data to help ensure alignment with:
- Study protocols
- Protocol amendments
- Applicable regulatory standards
- Internal data requirements
Assay Validation Support
The selected candidate will also support assay validation workflows and related processes as part of the assigned responsibilities.
This provides exposure to laboratory and study-related validation activities.
Digital Image Data Processing
Responsibilities may include supporting global digital image data operations, such as:
- Processing slide scans
- Managing associated metadata
- Supporting digital image data workflows
- Performing assigned data-related checks
Workload and Time Management
The position requires the ability to:
- Plan assigned work.
- Prioritize tasks.
- Manage multiple responsibilities.
- Complete activities within expected timelines.
- Develop effective time-management skills.
Cross-Functional Collaboration
The Data Associate I will work with:
- Cross-department teams
- Global teams
- Clinical research personnel
- Data-related functions
- Other business stakeholders as required
The role also includes participation in cross-functional training programs to develop technical knowledge and support business operations.
Training and Team Support
Depending on the assigned work, the employee may:
- Train or instruct less experienced staff on entry-level projects.
- Share knowledge related to assigned processes.
- Support team activities under appropriate supervision.
Additional administrative and related duties may be assigned according to business requirements.
Required Skills
Candidates should develop or demonstrate:
- Basic data management skills
- Attention to detail
- Ability to follow study protocols
- Data accuracy and quality awareness
- Time-management skills
- Ability to prioritize tasks
- Willingness to learn clinical research processes
- Ability to work with cross-functional teams
- Ability to work with global teams
- Basic computer and data-handling skills
- Ability to work under regular supervision
Clinical Research and Data Knowledge
The position provides exposure to several areas of clinical research and laboratory data operations, including:
- Clinical study protocols
- Toxicology study data
- Data acquisition systems
- Quality checks
- Regulatory requirements
- Assay validation
- Digital image data
- Metadata management
Work Location and Timings
- Location: Yeshwantpur, Bengaluru, Karnataka
- Job Type: Full Time
- Work Schedule: Rotating Shift
- Work Environment: Labcorp workplace in Bengaluru
The vacancy specifically mentions a rotating shift schedule.
Salary / CTC
Labcorp has not specified the salary or CTC for the Data Associate I position in the available vacancy information.
Candidates should confirm compensation and employment terms during the official recruitment process.
Selection Process
The detailed selection process has not been specified in the vacancy information.
Candidates may be evaluated based on their educational qualification, scientific background, ability to understand study protocols, attention to detail, data-handling capabilities and relevant clinical research exposure.
How to Apply for Labcorp Data Associate I
Interested and eligible candidates should submit their application through Labcorp’s official careers platform before the stated deadline.
Application Deadline
October 9, 2026
Candidates should complete their application before the listed closing date.
Important Details Before Applying
- The hiring company is Labcorp.
- The position is Data Associate I.
- The job location is Yeshwantpur, Bengaluru, Karnataka.
- This is a full-time position.
- The work schedule is rotating shift.
- A Bachelor’s Degree in Science is the minimum qualification.
- A Master’s Degree in Science is preferred.
- 6 months of clinical research industry experience is preferred.
- The role includes toxicology study data entry and quality checks.
- Candidates will support assay validation workflows.
- Digital image data processing and metadata management are also part of the role.
- The requisition ID is 2635233.
- The application deadline is October 9, 2026.
- Salary/CTC has not been disclosed.
Frequently Asked Questions
1. What is the job title at Labcorp?
The position is Data Associate I.
2. Where is the Labcorp Data Associate I job located?
The position is based at Yeshwantpur in Bengaluru, Karnataka.
3. What is the minimum educational qualification?
A Bachelor’s Degree in Science is required.
4. Is a Master’s degree preferred?
Yes. A Master’s Degree in Science is listed as a preferred qualification.
5. Is clinical research experience required?
The vacancy lists 6 months of clinical research industry experience as a preferred qualification.
6. Is this job suitable for freshers?
The minimum qualification is a Bachelor’s degree in Science, while prior clinical research experience is listed as preferred. Candidates without the preferred experience may review the official vacancy to determine their eligibility.
7. What type of data will the employee handle?
The role includes toxicology study data, manually collected data, database information and digital image data.
8. Does the role involve quality checking?
Yes. Basic quality checks and review of study data for protocol and regulatory compliance are part of the responsibilities.
9. Does this position involve rotating shifts?
Yes. The listed work schedule is rotating shift.
10. Does the job involve assay validation?
Yes. The Data Associate I will support assay validation workflows and processes.
11. What is the requisition ID?
The requisition ID is 2635233.
12. What is the application deadline?
The listed application deadline is October 9, 2026.
13. What is the salary for this position?
The salary or CTC has not been specified in the available vacancy information.
Important Note
Recruitment requirements, eligibility criteria, work schedules, application deadlines and other employment conditions may change. Candidates should verify the latest information on Labcorp’s official careers platform before applying and should rely on the employer’s official communication for final recruitment terms.