JIPMER Clinical Trial Coordinator Recruitment 2026

JIPMER is hiring 1 Clinical Trial Coordinator for its Clinical Trial Unit in the Department of Medical Oncology at Puducherry. If you have a B.Sc Nursing degree and can speak, read and write Tamil, you can attend the walk-in interview — no online application is needed. The interview is on 17 August 2026 at 9:00 AM. The post pays a consolidated Rs. 22,000 per month for a 1-year contract.

JIPMER Clinical Trial Coordinator Recruitment 2026 - 1 Post

The Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, has released a notification (Advt No. JIP/Med Onco/Trial Unit/JTC-2025-03) for 1 Clinical Trial Coordinator post under an externally funded research project titled "Clinical Trial Unit, Medical Oncology," led by Principal Investigator Dr. Biswajit Dubashi. This is a contract post for 1 year, and there is no separate online application — eligible candidates can walk in directly for the selection process.

JIPMER is one of India's premier autonomous medical institutions, offering multi-specialty patient care, medical education and research. Working as a Clinical Trial Coordinator here gives you direct exposure to structured, ethics-committee-monitored cancer research — valuable experience if you're a nursing graduate looking to build a career in clinical research. As a Coordinator, you'll play a key role in running cancer clinical trials — from enrolling patients and getting informed consent, to managing trial data and coordinating with the Ethics Committee. Since the project involves patients from the local community, the ability to communicate in Tamil is essential for this role.

Who Can Apply?

• Essential Qualification: A B.Sc Nursing degree with a minimum of Second Class or equivalent CGPA.
• Language: You must be able to speak, read and write Tamil, since the role involves direct communication with patients and the consent process.
• Desirable: Prior experience in clinical trials or working with cancer patients, strong communication skills, proficiency in computer operations, and GCP (Good Clinical Practice) training.

Age Limit

• The maximum age limit is 35 years, calculated as on the last date of receipt of applications.

Salary

• Selected candidates will get a consolidated remuneration of Rs. 22,000 per month.
• No other allowances are payable on top of this consolidated amount, and the pay may be revised from time to time at the discretion of the Principal Investigator.

Selection Process

JIPMER will shortlist candidates based on their application, CV and supporting documents, then conduct a written test followed by an interview:

1. Shortlisting: Based on details in your application form, CV, and documentary proof.
2. Written Test: Covers clinical trials, Good Clinical Practice (GCP) basics, cancer knowledge, chemotherapy handling, drug storage, and basic Excel/MS Word skills.
3. Interview: Covers your nursing knowledge, patient counseling ability, understanding of clinical research and GCP, communication skills and overall aptitude for the role.

Interviews may be held in person or via videoconferencing at the discretion of the Principal Investigator — if it's online, make sure you have a working device with camera, audio and a stable internet connection.

How to Apply

There is no online application form for this post. Follow these steps to apply:

1. Prepare your application in the prescribed format along with your CV and supporting documents — applications with only a CV and no proper form will be rejected.
2. Reach the Department of Medical Oncology, 3rd Floor, Super Specialty Block (SSB), JIPMER, Puducherry - 605006 by 9:00 AM on 17 August 2026.
3. Attend the written test and interview on the same day.
4. Keep a valid email ID and mobile number ready — both are compulsory for the process.

Important Dates

• Notification Date: 5 August 2026
• Walk-in Interview & Written Test Date: 17 August 2026
• Reporting Time: 9:00 AM

• Recruit and enroll patients into the clinical trial with proper informed consent
• Enter and manage patient data accurately in the trial database
• Assist with administration of investigational drugs and chemotherapy under supervision
• Maintain trial master files and ensure proper documentation
• Coordinate randomization processes for study participants
• Monitor and report adverse events during the trial
• Prepare and submit periodic reports to the Ethics Committee
• Conduct patient follow-up visits and check compliance with study protocols