PGIMER Careers: Apply Now for Project Research Scientist Position
PGIMER Careers: PGIMER Chandigarh is inviting applications for the position of Project Research Scientist-I (Medical) to support a multi-center, double-blinded randomized clinical trial funded by ICMR. This role is ideal for medical professionals who aspire to build a strong foundation in clinical research, patient management, trial coordination, and evidence-based medicine.
PGIMER Careers: Job Details
- Position: Project Research Scientist-I (Medical)
- Location: PGIMER, Chandigarh
- Post: 01
- Department: Internal Medicine
- Remuneration: ₹67,000 + HRA as per rules
About PGIMER
The Postgraduate Institute of Medical Education & Research (PGIMER), Chandigarh, is one of India’s premier medical and research institutions. Recognised for its advanced tertiary care, cutting-edge research, and high academic standards, the institute conducts numerous nationally funded clinical and translational research projects. PGIMER continues to lead innovation in medical science through its multidisciplinary teams, robust infrastructure, and commitment to evidence-based healthcare.
PGIMER Careers: Eligibility & Qualifications
Essential Qualifications
- MBBS/BDS or higher medical qualification
- Completion of compulsory 1-year internship
- Valid registration with the State Medical Council
- Ability to converse fluently in English and Hindi
Desirable Qualifications
- Prior clinical research experience after MBBS
- GCP (Good Clinical Practice) certification
- Working knowledge of MS Word, Excel, PowerPoint, and REDCap
- Ability to communicate in Punjabi
Age Limit
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Maximum: 35 years (as of the last date of application)
Role Overview
The Project Research Scientist-I will support all operational, clinical, and administrative components of a major ICMR-funded randomized controlled trial. The role involves patient screening, recruitment, follow-ups, trial documentation, coordination with multiple centres, and ensuring adherence to research protocols and ethical standards.
Key Responsibilities
Clinical & Research Responsibilities
- Screen eligible patients and obtain informed consent
- Recruit subjects as per trial criteria
- Perform daily clinical assessments and document findings
- Conduct follow-up assessments and ensure protocol compliance
- Assist with outcome data collection and reporting
Trial Coordination & Administration
- Maintain regular communication with ICMR and collaborating sites
- Handle data entry, documentation, and REDCap updates
- Support grant management and financial tracking
- Submit reports to the Ethics Committee as required
- Prepare case records, logs, and trial-related documents
General Responsibilities
- Ensure quality and integrity of trial data
- Maintain patient confidentiality and ethical conduct
- Complete any additional tasks assigned by the principal investigator.
How to Apply
- Eligible candidates must apply online only through the following Google Form link
- Applications submitted in any other format (email/handwritten/offline) will not be accepted.
- Last date for submission: 22 December 2025, 23:59 PM
- Selected/shortlisted candidates will be informed through email for further interview/assessment.
