Labcorp is hiring for the position of Informed Consent Codification Associate I at its Bengaluru, India location. Candidates with a Bachelor’s degree in Science and at least 6 months of experience in writing, reviewing, or reading informed consent documents for clinical trials are eligible to apply.
The role involves informed consent codification, quality checks, error identification, troubleshooting, and maintaining compliance with standard operating procedures (SOPs) and validation standards.
Job Details
| Particulars | Details |
|---|---|
| Company | Labcorp |
| Job Role | Informed Consent Codification Associate I |
| Job ID | 2638127 |
| Job Location | Brigade Twin Tower, Bengaluru, India |
| Job Type | Full Time |
| Qualification | Bachelor’s Degree in Science |
| Experience | 6 Months |
| Work Schedule | Monday–Friday, Rotating Shift |
| Preferred Qualification | Master’s Degree in Science |
| Preferred Technical Skills | SQL and Python |
| Last Date to Apply | November 9, 2026 |
| Application Mode | Online |
Positions
- Informed Consent Codification Associate I
Job Responsibilities
Selected candidates will be responsible for informed consent codification and related quality and compliance activities.
Key responsibilities include:
- Perform informed consent codification across multiple client instances.
- Ensure informed consent codification activities are completed correctly.
- Meet project delivery schedules.
- Identify errors through troubleshooting and analytical skills.
- Triage unacceptable errors and support resolution.
- Maintain knowledge of SOPs and validation work procedures.
- Follow applicable standards related to the System Development Life Cycle (SDLC).
Eligibility and Qualifications
Minimum Educational Qualification:
- Bachelor’s degree in Science.
Minimum Experience:
- At least 6 months of experience in writing, reviewing, or reading informed consent documents for clinical trials.
Preferred Qualification:
- Master’s degree in Science.
Preferred Technical Experience:
- 6 months of experience with programming languages and tools such as SQL and Python.
Required Skills and Expertise
Candidates should possess the following skills:
- Knowledge of informed consent forms.
- Understanding of global regulations and guidance documents related to informed consent.
- Problem-solving and logical reasoning skills.
- Strong analytical and troubleshooting abilities.
- Proficiency in Microsoft Office, particularly Excel and Word.
- Strong written and verbal communication skills.
- Good interpersonal skills.
- Ability to plan, prioritize, and manage work in a fast-paced environment.
- Attention to detail and process optimization.
- Understanding of data integrity.
- Experience with 21 CFR Part 11 in the pharmaceutical, biotechnology, CRO, or related industry.
