- Contract-based research position for a 5-year project titled Post-operative intraperitoneal chemotherapy after interval cytoreduction in epithelial ovarian cancer (POICE 2024) funded by the National Cancer Grid.
- Location: JIPMER, Puducherry (on-site coordination for a multicenter trial).
- Key responsibilities: Coordinating the project at JIPMER, developing/maintaining the Electronic Case Report Form (ECRF), ensuring Good Clinical Practice (GCP) compliance, monitoring recruitment across centers, training staff, and managing financial aspects.
- Project Investigator: Prasanth Ganesan (Medical Oncology Department).
JIP
Active Listing
🎓 Master's Degree
🎓 Ph.D.
Project Research Scientist I (PRS I) – Multicenter Clinical Trial Recruitment
Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER)
Total Vacancies
1
Job Location
JIPMER, Puducherry-605006 (Dept. of Medical Oncology, RCC annex)
Apply Deadline
28 Sep 2026
📋 Recruitment Overview
| Organization | Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) (JIPMER) |
| Job Category | Medical |
| Eligibility Qualification | Master's Degree (masters-degree), Ph.D. (phd) |
| Number of Vacancies | 1 Posts |
| Salary / Pay Scale | ₹66,080 - ₹66,080 Per Month |
| Age Limits | Maximum 35 Years |
| Gender Eligibility | both |
| Experience Required | • Minimum Years: 2, Field: clinical trials or clinical research, Proof Required: letter from previous employer |
| Application Fee | • Summary: No explicit mention of an application fee is provided in the raw job notification text. |
📄 Details & Description
🎓 Eligibility Criteria
- Essential Qualifications:
First Class Postgraduate Degree OR Second Class PG Degree with a PhD.
Minimum 2 years of experience in conducting clinical trials or clinical research (proof required via letter from previous employer).
Good Clinical Practice (GCP) Certification (proof required).
- Desirable Qualifications:
Experience in multicenter trials or pharma-sponsored trials.
Ability to create databases using programs like epicollect/RedCap.
Experience in monitoring clinical trial projects.
Prior work in cancer trials.
Experience in writing protocols, regulatory submissions, or IEC documents.
First Class Postgraduate Degree OR Second Class PG Degree with a PhD.
Minimum 2 years of experience in conducting clinical trials or clinical research (proof required via letter from previous employer).
Good Clinical Practice (GCP) Certification (proof required).
- Desirable Qualifications:
Experience in multicenter trials or pharma-sponsored trials.
Ability to create databases using programs like epicollect/RedCap.
Experience in monitoring clinical trial projects.
Prior work in cancer trials.
Experience in writing protocols, regulatory submissions, or IEC documents.
⚙️ Selection Process
- Shortlisting based on application, CV, and documentary proof.
- Written test covering:
Basics of Clinical Research and Oncology.
Clinical Trial Design and Conduct.
Clinical Trial Data Management and Analysis.
Ethics, GCP, and Aptitude.
- Interview by a panel of experts assessing:
Knowledge of clinical research/GCP.
Communication skills.
* Aptitude for the role.
- Written test covering:
Basics of Clinical Research and Oncology.
Clinical Trial Design and Conduct.
Clinical Trial Data Management and Analysis.
Ethics, GCP, and Aptitude.
- Interview by a panel of experts assessing:
Knowledge of clinical research/GCP.
Communication skills.
* Aptitude for the role.
🏷️ Category Eligibility & Reservations
All
📂 Required Documents
- Filled prescribed application form (attached).
- Curriculum Vitae (CV).
- Scanned supporting documents (all in one PDF file).
- Proof of GCP Certification.
- Letter from previous employer confirming nature of work (for experience validation).
- Curriculum Vitae (CV).
- Scanned supporting documents (all in one PDF file).
- Proof of GCP Certification.
- Letter from previous employer confirming nature of work (for experience validation).
💳 Application Fee Details
• Summary: No explicit mention of an application fee is provided in the raw job notification text.
❓ Frequently Asked Questions
Q.
What is the last date to apply for the Project Research Scientist I (PRS I) position at JIPMER?
The last date to submit applications is 28th September 2026 at 10:00 PM via email to nocirecruitment@gmail.com.
Q.
What is the maximum age limit for applicants applying for the PRS I role?
The maximum age limit for applicants is 35 years as of the last date of receipt of applications (28th September 2026).
Q.
Is there an application fee for the JIPMER PRS I recruitment?
No, there is no application fee for this recruitment.
Q.
What is the expected joining date for the selected candidate?
The selected candidate is expected to join on 5th October 2026 to commence work on the ongoing multicenter trial.
Q.
What is the consolidated salary for the Project Research Scientist I (PRS I) position?
The consolidated salary is Rs. 66,080 per month, including HRA. No additional allowances are provided.