Informed Consent Codification Associate

Labcorp

Bengaluru, Karnataka, India0–2 yrs3h agovia LinkedIn

This job at a glance

Who can apply
Freshers and up to 2 years · Bachelor's degree or Master's degree
Must know
TroubleshootingPatient careExcel
Nice to have
PythonSQL
Work
On-site in Bengaluru
Pay
Not stated by the employer.
Skill demand
Patient care39%Excel15%Python10%Troubleshooting6%of 100 similar fresher jobs posted in India this week
Listed
4 Nov 2026 · still open

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About the Role

Labcorp is seeking an Informed Consent Codification Associate I to join their team in Bangalore, India. This role involves working a Monday - Friday rotating shift schedule.

Key Responsibilities

  • Perform informed consent codification across multiple client instances.
  • Ensure informed consent codification is executed correctly and to completion.
  • Meet delivery schedules.
  • Utilize strong troubleshooting and analytical skills for error identification and resolution.
  • Triage unacceptable errors for resolution.
  • Maintain and utilize strong knowledge of SOPs and validation work procedures/standards in relation to the System Development Life Cycle.

Requirements & Tech Stack

  • Bachelor's degree in science.
  • 6 months of experience in writing, reviewing, or reading informed consent for clinical trials.
  • Problem Solving/Logic Skills.
  • Strong communication and interpersonal skills.
  • Strong MS/Office skills, particularly with Excel and Word.
  • Proven ability to plan, prioritize, and manage in a fast-paced environment with a high degree of initiative.
  • Strong drive for process optimization and data integrity.
  • Excellent communication and interpersonal skills with great attention to detail.

Qualifications

  • Master's degree in science (Preferred).
  • 6 months of experience in programming languages and tools such as SQL and Python (Preferred).
  • Knowledge of informed consent forms.
  • Knowledge of global regulation and guidance documents in relation to informed consent information.
  • Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO, or related industry.

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