AIIMS Project Nurse III GRASPP Recruitment 2026

AIIMS Project Nurse III GRASPP Recruitment 2026: Overview

All India Institute of Medical Sciences (AIIMS), New Delhi is recruiting a Project Nurse, equivalent to Project Nurse-III, through its Department of Obstetrics and Gynaecology. The role belongs to the GRASPP study on screening and prevention of placental disorders, under project code I-1899. Although AIIMS is handling recruitment, your work location is ESIC, Faridabad.

GRASPP is a randomised controlled trial evaluating a two-step contingent screening strategy for Great Obstetric Syndrome. This is a temporary project engagement connected with the study and its participants, including antenatal and infant follow-up.

Service Conditions and Caveats

• Initial appointment: The engagement starts with a three-month term. The notice describes a possible six-month extension within the project duration, depending on satisfactory performance.
• Employment status: This project appointment does not give you a claim to a regular AIIMS position. The temporary nature of the engagement remains an important condition of accepting the role.
• Work setting: You should be ready for a round-the-clock roster supporting continuous study operations. The notice also includes home visits for antenatal and infant data collection when needed.
• Travel support: The notice does not provide travel or daily allowance for this recruitment.
• Application completeness: Late, delayed, incomplete or unsigned applications will be rejected without further correspondence.

Application Submission Notes

Send your application by email to jobrecruitmentaiims@gmail.com. The subject line must clearly identify Project Nurse-III and I-1899, so the team can connect your application to this study.

Email communication: The department will share interview arrangements only with shortlisted applicants. Check the email account you use for your application for the interview date, time and mode.

• Screen participants and obtain their written informed consent.
• Collect clinical data at enrolment, follow-up visits and delivery, and complete case report forms.
• Assist doctors with clinical examinations and study procedures.
• Measure vital signs and body measurements.
• Counsel participants about study requirements and follow-up visits.
• Report missed infant follow-up visits to the clinical research officer.
• Conduct home visits for antenatal and infant data collection when needed.
• Collect study samples, particularly during deliveries, and work on the round-the-clock roster.