Labcorp has announced a new opportunity for candidates interested in building a career in clinical research and clinical trial operations. The company is hiring for the position of Informed Consent Codification Associate in Bengaluru, Karnataka.
This Labcorp hiring opportunity is particularly relevant for candidates with a Bachelor’s degree in Science, while candidates holding a Master’s degree in Science are preferred. The role involves informed consent codification, data integrity, troubleshooting, SOP compliance and working with clinical trial informed consent documentation.
Candidates with knowledge of informed consent forms (ICFs), SQL, Microsoft Excel, 21 CFR Part 11 and clinical research regulations may be particularly suited to this position.
Labcorp Job Overview
| Particular | Details |
|---|---|
| Company | Labcorp |
| Position | Informed Consent Codification Associate |
| Related Role Mentioned | Centralized Study Associate II |
| Job Location | Bengaluru, Karnataka, India |
| Job Type | Full-Time |
| Work Schedule | Monday–Friday, Rotating Shift |
| Qualification | Bachelor’s Degree in Science |
| Preferred Qualification | Master’s Degree in Science |
| Job Requisition ID | 2628941 |
| Application Deadline | August 31, 2026 |
About the Role
The Informed Consent Codification Associate at Labcorp will support informed consent codification activities across multiple client instances. The position requires accuracy, analytical ability and familiarity with clinical trial documentation and applicable procedures.
The associate will be expected to complete informed consent codification correctly and within defined delivery timelines while identifying and resolving errors.
Key Responsibilities
- Perform informed consent codification across multiple client instances.
- Ensure informed consent codification activities are completed accurately.
- Meet established project and delivery schedules.
- Identify errors using strong analytical and troubleshooting skills.
- Triage unacceptable errors and support their resolution.
- Follow applicable SOPs, validation procedures and work standards.
- Maintain knowledge of procedures associated with the System Development Life Cycle (SDLC).
- Support high standards of process optimization and data integrity.
- Work with clinical trial informed consent documentation according to applicable procedures and regulations.
Qualification & Eligibility
Minimum Qualification
Candidates should possess a:
Bachelor’s degree in Science
Preferred Qualification
A Master’s degree in Science is preferred.
The official job description does not specify a particular science specialization. Therefore, candidates should assess whether their academic background and skills align with the clinical research and informed consent requirements before applying.
Skills Required
Candidates should preferably possess:
- Strong problem-solving and logical reasoning skills
- Excellent communication and interpersonal skills
- Working knowledge of SQL
- Strong Microsoft Office skills, particularly Excel and Word
- Knowledge of Informed Consent Forms (ICFs)
- Understanding of clinical trial informed consent documentation
- Knowledge of global regulations and guidance related to informed consent
- Strong attention to detail
- Understanding of data integrity principles
- Knowledge or experience with 21 CFR Part 11
- Ability to work in pharmaceutical, biotechnology, CRO or related regulated environments
- Strong analytical and troubleshooting capabilities
Preferred Clinical Research Knowledge
Experience writing, reviewing or reading informed consent forms for clinical trials can be valuable for this Labcorp job.
Knowledge of global informed consent regulations, clinical research documentation, SOPs, validation standards and 21 CFR Part 11 can also strengthen a candidate’s profile.
Why Consider This Labcorp Opportunity?
This position offers exposure to an important component of clinical research—informed consent management and codification. Professionals in this role can develop experience involving clinical trial documentation, regulatory requirements, data quality and validated systems.
Potential professional benefits include:
- Exposure to global clinical research processes
- Experience with informed consent documentation
- Opportunity to work in a regulated life sciences environment
- Development of clinical research data and compliance skills
- Exposure to SOPs and validation processes
- Experience working with data integrity requirements
- Career development within a global life sciences organization
Who Should Apply?
This opportunity may be relevant for science graduates who have knowledge or experience in areas such as:
Clinical Research | Clinical Trial Operations | Informed Consent Forms | Clinical Data | Life Sciences | Pharmaceutical Industry | Biotechnology | CRO Operations
Applicants should carefully review the official eligibility criteria before submitting their application.
How to Apply
