ILBS Recruitment – Clinical Research Coordinator | Clinical Research Jobs 2025
If you are looking for high-impact clinical research jobs in India, this latest ILBS recruitment is an opportunity you cannot miss. ILBS is conducting a walk-in interview for a Clinical Research Coordinator role under a prestigious Boehringer Ingelheim-funded Phase III clinical trial. This opening is ideal for ambitious candidates seeking growth in clinical research jobs, advanced clinical trials, and real-world translational research.
About the Institute (ILBS):
The Institute of Liver and Biliary Sciences (ILBS), New Delhi, is a globally recognised research-driven institute dedicated to liver diseases, hepatobiliary sciences, and advanced clinical care. Known for its robust clinical research jobs ecosystem and cutting-edge infrastructure, ILBS regularly collaborates with international agencies and industry partners.
Recruitment Notice:
- Walk-In Interview for the Post of Clinical Research Coordinator
- Project funded by Boehringer Ingelheim
- Project Title: Phase III double-blind, randomized, placebo-controlled trial evaluating liver-related outcomes and safety of once-weekly Survodutide in NASH/MASH cirrhosis patients
- Protocol Number: 1404-0064
Available Position:
- Role: Clinical Research Coordinator
- Number of Vacancies: 01
- Funding Agency: Boehringer Ingelheim
- Duration: 4.5 Years
- Location: ILBS, Vasant Kunj, New Delhi
Job Overview:
This position under ILBS recruitment involves coordinating a major Phase III clinical trial on NASH/MASH cirrhosis. This role is ideal for candidates looking for hands-on exposure in clinical research jobs, data management, regulatory compliance, patient interaction, and trial execution.
Essential Qualifications:
- First-class Master’s in Clinical Research/Clinical Trials (including integrated master’s), OR
- Second-class Master’s in Clinical Research/Clinical Trials with a PhD in Clinical Research / Clinical Trials / Epidemiology
Desirable:
- 1–2 years of experience in clinical trials
- Experience in patient recruitment, documentation, and protocol adherence
Age Limit:
- Maximum 35 years
Remuneration:
- ₹45,000 (Consolidated)
Key Responsibilities:
- Coordinating day-to-day clinical trial activities
- Ensuring compliance with GCP, ICH, and project protocols
- Managing patient visits, sample collection, follow-ups
- Maintaining clinical trial documentation and CRFs
- Working closely with investigators and trial teams
- Supporting data entry, monitoring, and reporting
Skills Required:
- Strong understanding of clinical trial protocols
- Excellent communication and patient-handling skills
- Ability to work in regulated environments
- Knowledge of GCP guidelines
- Record-keeping and documentation accuracy
Important Dates:
- Walk-In Interview: 21st Nov 2025
- Time: 11:00 AM – 1:00 PM
- Venue: MPH Phase II, 1st Floor, ILBS, D-1, Vasant Kunj, New Delhi – 110070
General Terms & Conditions:
- Appointment is contractual, with a 1-year probation
- No TA/DA provided for attending the walk-in
- Eligibility and age calculated as of 31.10.2025
- Jurisdiction: Delhi/New Delhi only
