Labcorp has announced two new job openings in Bengaluru for candidates interested in clinical research, clinical data management, and life sciences careers. The company is recruiting for Data Management Associate I and Informed Consent Codification Associate positions at its Yeswanthpura, Bengaluru facility.

These Labcorp jobs in Bangalore are particularly relevant for candidates with a Bachelor’s or Master’s degree in Science who want to build a career in clinical data management, clinical research operations, data integrity, or informed consent management.

According to the official job descriptions, current or prior Labcorp internship experience is listed under the minimum qualifications for both positions. Candidates should carefully review this requirement before applying.

The application deadline for both Labcorp Bengaluru jobs is August 18, 2026.

Role 1: Data Management Associate I

Job Title: Data Management Associate I
Company: Labcorp
Location: Yeswanthpura, Bengaluru, Karnataka
Requisition ID: 2626461
Employment Type: Full-Time
Work Schedule: Monday-Friday, 2:00 PM-11:00 PM (Second Shift)
Application Deadline: August 18, 2026

Job Overview

The Data Management Associate I at Labcorp will support data feed configurations, data point mapping development, quality control, troubleshooting, and data management activities.

This position requires candidates to work accurately with data, follow SOPs and validation standards, identify errors and omissions, and contribute to continuous process improvement.

Key Responsibilities

• Manage multiple data feed configuration and data point mapping activities.
• Plan and establish timelines to meet business expectations.
• Perform QC of data feed configurations and data point mappings.
• Identify errors and omissions through strong troubleshooting and analytical skills.
• Complete mandatory Quality Assurance training.
• Attend required Data Management meetings.
• Participate in job shadowing and interdepartmental development opportunities.
• Complete training related to process and system changes.
• Participate in advanced training for continued professional development.
• Contribute to training and development of assigned team members.
• Apply knowledge of SOPs, validation standards, and work procedures.
• Identify opportunities for process improvement.
• Provide guidance and training to staff when required.

Minimum Qualifications

Candidates should have:

• Bachelor’s degree in Science
• Current or prior Labcorp internship experience

Preferred Qualifications

Labcorp lists the following as preferred:

• Approximately 6 months of experience in the contract research industry
• Master’s degree in Science

Skills Required

Candidates should have or develop competency in:

• SQL
• Microsoft Excel
• Microsoft Word
• Database query tools
• MySQL Workbench
• DB Forge
• Data mapping
• Data quality control
• Data validation concepts
• SOP compliance
• Troubleshooting
• Logical and analytical thinking
• Problem solving
• Communication and interpersonal skills
• Attention to detail

Role 2: Informed Consent Codification Associate

Job Title: Informed Consent Codification Associate
Company: Labcorp
Location: Yeswanthpura, Bengaluru, Karnataka
Requisition ID: 2624228
Employment Type: Full-Time
Work Schedule: Monday-Friday, Rotating Shift
Application Deadline: August 18, 2026

Important JD Note: The vacancy heading supplied by Labcorp is Informed Consent Codification Associate, while the job description states that Labcorp is seeking a Centralized Study Associate II. Applicants should verify the final position title on the official application portal before submitting their application.

Job Overview

The Informed Consent Codification Associate job at Labcorp focuses on informed consent codification, data quality, troubleshooting, SOP compliance, validation procedures, and clinical trial documentation.

The position is relevant to candidates interested in clinical research, informed consent forms, clinical trial regulations, data integrity, and regulated clinical systems.

Key Responsibilities

• Perform informed consent codification across multiple client instances.
• Ensure informed consent codification is completed accurately.
• Meet required delivery schedules.
• Identify errors through troubleshooting and analytical review.
• Determine appropriate resolution steps for identified issues.
• Triage unacceptable errors for resolution.
• Maintain strong knowledge of SOPs.
• Follow validation work procedures and standards.
• Work according to requirements associated with the System Development Life Cycle (SDLC).

Minimum Qualifications

Candidates should have:

• Bachelor’s degree in Science
• Current or prior Labcorp internship experience

Preferred Qualifications

• Master’s degree in Science

Preferred Knowledge and Skills

Candidates should ideally possess knowledge or exposure to:

• Informed Consent Forms (ICFs)
• Clinical trials
• Clinical research documentation
• Global regulations and guidance related to informed consent
• SQL
• Microsoft Excel
• Microsoft Word
• SOPs
• Validation standards
• System Development Life Cycle
• Data integrity
• Process optimization
• 21 CFR Part 11
• Pharmaceutical, biotechnology, CRO, or related environments
• Problem-solving and logical reasoning
• Strong attention to detail

Experience in writing, reviewing, or reading informed consent forms for clinical trials is particularly relevant to this position.

Who Can Apply for Labcorp Jobs?

Based strictly on the supplied Labcorp job descriptions, the minimum educational qualification for both vacancies is a Bachelor’s degree in Science, while a Master’s degree in Science is preferred.

Candidates from relevant science and life sciences educational backgrounds may review the official posting to determine whether their specific degree is accepted.

However, applicants should pay particular attention to one requirement: current or prior Labcorp internship experience is explicitly listed as a minimum qualification for both roles.

For the Data Management Associate I position, approximately six months of contract research industry experience is preferred but is not listed as the minimum experience requirement.

Why Consider These Labcorp Opportunities?

These positions can provide exposure to important functions within clinical research and data management, including:

• Clinical data management processes
• Data feed configuration and mapping
• Quality control and validation
• SQL and database environments
• SOP-driven operations
• Clinical trial informed consent documentation
• Data integrity principles
• 21 CFR Part 11 concepts
• System Development Life Cycle procedures
• Cross-functional clinical research operations

Labcorp is a global laboratory services organization working across diagnostics, drug development, clinical research, healthcare data, and laboratory services. These positions provide an opportunity to work within a regulated healthcare and clinical research environment.

How to Apply

Application Link For Data Management Associate I

Application Link For Informed Consent Codification Associate | Centralized Study Associate