Scientist Job Opportunity at AIIMS New Delhi for Medical Professionals
The scientist job opening at AIIMS New Delhi offers a valuable opportunity for medical professionals looking to build a career in clinical research. Released under the latest AIIMS recruitment, this role is ideal for qualified doctors seeking MBBS jobs in government research projects focused on maternal health and hypertensive disorders in pregnancy.
Job Details:Â
- Job Position: Project Research Scientist-I (Medical)
- Number of Posts: One
- Job Location: AIIMS New Delhi – Ansari Nagar, New Delhi – 110029
- Monthly Salary: Rs. 67,000 + 30% HRA = Rs. 87,100/-
- Age Limit: Maximum 35 years
- Last Date to Apply: 06th January 2025
About the Institute:
The All India Institute of Medical Sciences (AIIMS), New Delhi, located at Ansari Nagar, is one of India’s most prestigious government medical institutions. Known for excellence in healthcare, education, and research, AIIMS New Delhi regularly announces opportunities through AIIMS recruitment for doctors and researchers. This scientist’s job is offered under the Department of Obstetrics and Gynecology for a nationally important research project.
Scientist Job Qualifications:
Essential:
-
MBBS / BDS or equivalent
Desirable:
- Experience in clinical research studies or related fields
- Excellent reading comprehension, writing, and verbal communication skills
- Computer proficiency, including Microsoft Office applications
- Ability to develop and implement clinical monitoring plans, SOPs, and database concepts
- Effective time management and multitasking skills
- Ability to maintain professional working relationships with investigators and team members
Project Details:
- Project Title: Center for Advanced Research in Hypertensive Disorders in Pregnancy
- Institute Name: All India Institute of Medical Sciences (AIIMS), New Delhi
- Department: Obstetrics and Gynecology
- Project Duration: 60 months
Scientist Job – Key Responsibilities:
The selected candidate for this scientist job will be responsible for:
- Supervision and coordination of clinical activities at the assigned study site
- Obtaining written informed consent in compliance with ethical standards
- Ensuring accurate, complete, and timely data collection and documentation
- Resolving site-level queries efficiently
- Tracking project progress, safety reporting, and timelines
- Monitoring deliverables and ensuring regulatory compliance
- Reviewing and verifying CRFs before submission to the data management team
- Ensuring follow-up visits and related data collection
- Coordinating data flow from collection to electronic data entry platforms
- Training research assistants and field workers for newborn data collection and follow-ups
- Performing any additional duties assigned by the Principal Investigator
