The Institute of Liver and Biliary Sciences (ILBS), New Delhi, has announced a walk-in interview for the post of Clinical Research Coordinator under a clinical research project funded by Boehringer Ingelheim.
The selected candidate will work on a Phase III clinical trial evaluating the long-term efficacy and safety of Survodutide weekly injections in adult participants with non-cirrhotic NASH/MASH and F2–F3 stage liver fibrosis.
There is 1 vacancy for the Clinical Research Coordinator position. Eligible candidates can attend the walk-in interview on 30 September 2026 at ILBS, Vasant Kunj, New Delhi.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Research Coordinator |
| Vacancy | 01 |
| Funding Agency | Boehringer Ingelheim |
| Project Duration | 6.5 Years |
| Location | ILBS, Vasant Kunj, New Delhi |
| Remuneration | ₹45,000 per month (Consolidated) |
| Employment Type | Contract Basis |
| Probation | Initial 1 year |
| Age Limit | 35 years |
| Interview Mode | Walk-in, In Person |
| Interview Date | 30 September 2026 |
| Interview Time | 10:30 AM to 12:00 PM |
About the Clinical Trial Project
The Clinical Research Coordinator will be associated with Protocol Number 1404-0044, a randomized, double-blind, placebo-controlled, multicentre Phase III clinical trial.
Project Title
“A Randomized, double-blind, placebo-controlled, multicentre, Phase III trial evaluating long-term efficacy and safety of Survodutide weekly injections in adult participants patients with non-cirrhotic non-alcoholic steatohepatitis/metabolic associated steatohepatitis (NASH/MASH) and (F2) – (F3) stage of liver fibrosis.”
The project is funded by Boehringer Ingelheim and has a stated duration of 6.5 years.
Clinical Research Coordinator Responsibilities
The detailed day-to-day responsibilities are not separately specified in the recruitment notice. Based on the Clinical Research Coordinator role within a Phase III clinical trial, responsibilities may include:
- Supporting the day-to-day coordination of clinical trial activities.
- Assisting with participant screening, enrolment and follow-up.
- Maintaining clinical trial documentation and study records.
- Coordinating with investigators, study staff and other clinical research teams.
- Supporting protocol compliance and study procedures.
- Assisting with collection and maintenance of study-related data.
- Supporting regulatory and institutional documentation requirements.
- Maintaining appropriate trial records and essential documents.
- Coordinating scheduled study visits and related activities.
- Supporting the overall execution of the clinical research protocol.
Candidates should refer to the official recruitment notice and project requirements for the precise scope of duties.
Eligibility Criteria
Candidates must meet the specified educational qualifications and age criteria as of 31 August 2026.
Essential Qualification
Candidates must have either:
Option 1:
First-class Master’s degree in Clinical Research / Clinical Trials, including an integrated Master’s degree.
OR
Option 2:
Second-class Master’s degree in Clinical Research / Clinical Trials, including an integrated Master’s degree, with a PhD in Clinical Research / Clinical Trials / Epidemiology.
Desirable Experience
Candidates with 1–2 years of post-qualification experience in clinical trials are desirable.
Age Limit
The maximum age limit is 35 years.
The effective date for determining the required qualification, experience and upper age limit is 31 August 2026.
Salary and Benefits
The selected candidate will receive:
- ₹45,000 per month consolidated remuneration
- Opportunity to work on a Phase III clinical trial
- Exposure to clinical research activities in a specialized liver and biliary sciences institute
- Association with a project funded by Boehringer Ingelheim
- Project duration of 6.5 years, subject to the applicable project and contractual conditions
The appointment is on a contract basis and includes an initial one-year probation period.
Walk-In Interview Details
Eligible candidates are required to attend the interview in person.
Date: 30 September 2026
Reporting/Interview Time: 10:30 AM to 12:00 PM
Venue: MPH Phase II, 1st Floor,
Institute of Liver and Biliary Sciences (ILBS),
D-1, Vasant Kunj,
New Delhi – 110070
Candidates should arrive within the specified interview timing.
Documents Required
Candidates attending the Clinical Research Coordinator walk-in interview should bring:
- Complete application form
- Original educational qualification certificates
- Photocopies of degree/certificate/diploma
- Relevant testimonials
- Documents supporting professional experience, where applicable
Candidates should ensure that they meet all eligibility requirements before attending the interview.
How to Apply
Interested and eligible candidates can apply by attending the walk-in interview in person at ILBS on 30 September 2026 between 10:30 AM and 12:00 PM.