Clinical Research Job at Labcorp Bangalore
Looking for a promising Clinical Research Job in Bangalore? Labcorp is hiring a Centralized Study Associate II – Informed Consent Codification Associate for its clinical research team. This opportunity is ideal for science graduates and postgraduates who want to build a career in clinical trials, regulatory documentation, and healthcare research. Explore exciting Labcorp Careers and join a global organization working at the intersection of science, technology, and patient health.
About Labcorp
Labcorp is a global leader in laboratory services, diagnostic testing, and drug development solutions. The organization supports healthcare providers, pharmaceutical companies, researchers, and patients by delivering scientific insights that improve healthcare outcomes. With advanced technologies, innovative digital solutions, and a worldwide laboratory network, Labcorp contributes to some of the most important healthcare advancements globally. Through Labcorp Careers, professionals can work on meaningful projects that improve health and improve lives.
Job Details:
- Job Title: Informed Consent Codification Associate II
- Company: Labcorp
- Category: Clinical
- Location: Bengaluru, Karnataka, India
- Job ID: 2624236
- Employment Type: Full-Time
- Work Mode: On-Site
Role Overview
Labcorp is seeking an Informed Consent Codification Associate II to support clinical research operations by performing informed consent codification activities across multiple client studies. The role involves ensuring accurate and timely codification of informed consent data, maintaining data integrity, troubleshooting errors, and adhering to standard operating procedures (SOPs) and regulatory requirements within a clinical research environment.
The position requires strong analytical abilities, attention to detail, knowledge of informed consent documentation, and familiarity with clinical trial regulations and electronic data systems.
Key Responsibilities
- Perform informed consent codification activities across multiple client projects and study instances.
- Ensure informed consent codification tasks are completed accurately and within defined timelines.
- Identify, analyze, and resolve coding discrepancies and system-related issues.
- Apply strong troubleshooting and analytical skills to investigate errors and determine appropriate resolution steps.
- Escalate and manage unacceptable errors through appropriate resolution workflows.
- Maintain comprehensive knowledge of SOPs, validation procedures, and System Development Life Cycle (SDLC) standards.
- Ensure compliance with data integrity requirements and process optimization initiatives.
- Support quality-focused clinical data management activities.
- Maintain accurate documentation and follow established clinical research processes.
Required Qualifications
- Bachelor’s degree in Science or a related discipline.
Preferred Qualifications
- Master’s degree in Science or a related field.
- Experience in clinical research, pharmaceutical, biotechnology, or Contract Research Organization (CRO) environments.
Technical Skills & Knowledge
- Knowledge of informed consent forms and clinical trial documentation.
- Experience in writing, reviewing, or interpreting informed consent documents for clinical studies.
- Understanding of global regulations and guidance documents related to informed consent requirements.
- Working knowledge of SQL.
- Proficiency in Microsoft Office applications, particularly:
- MS Excel
- MS Word
- Familiarity with 21 CFR Part 11 compliance requirements in regulated industries.
- Understanding of electronic systems, validation processes, and data integrity principles.
Key Competencies
- Strong analytical and problem-solving skills.
- Excellent attention to detail and accuracy.
- Ability to identify issues and implement effective solutions.
- Strong communication and interpersonal skills.
- Ability to work collaboratively in a clinical research environment.
- Commitment to process improvement and maintaining high-quality standards.
- Ability to manage priorities and meet project deadlines.
Work Schedule
- Monday to Friday
- Rotational shifts
