The Society for Applied Studies (SAS), a reputed Delhi-based not-for-profit research organization, has announced a vacancy for a Clinical Research Coordinator to join an ongoing ICMR-funded clinical research study. This opportunity is ideal for candidates with experience in antenatal care, clinical trials, and hospital-based research coordination.
The position is based at Lady Hardinge Medical College (LHMC), Paharganj, New Delhi, and involves active participation in a public health study aimed at preventing preterm birth in at-risk pregnant women.
This role offers hands-on exposure to clinical trial coordination, adverse event reporting, data management, and participant follow-up, making it a valuable career opportunity in clinical research.
Job Overview
- Position: Clinical Research Coordinator
- Organization: Society for Applied Studies (SAS)
- Location: Lady Hardinge Medical College & Paharganj, New Delhi, India
- Project Type: ICMR-Funded Clinical Research Study
- Positions Available: 1
- Employment Type: Full-Time
Key Responsibilities
The Clinical Research Coordinator will:
- Coordinate between hospital teams and the study team for adverse event reporting
- Ensure proper participant care and clinical follow-up
- Manage data collection, documentation, and record maintenance
- Maintain study registers, logistics, and inventory management
- Develop and execute field visit schedules
- Summarize field observations and escalate issues promptly
- Assist in reporting of serious adverse events (SAEs)
- Perform additional study-related activities as assigned by the supervisor
This position requires strong coordination skills, regulatory awareness, and familiarity with clinical trial operations in antenatal and obstetric settings.
Eligibility Criteria
Educational Qualification
- Bachelor’s degree in Allied Medical Speciality:
- BDS
- BSc
- B.Pharm
- PLUS MPH or MSc (Clinical Trials)
Essential Requirements
- Minimum 1 year of relevant field experience in:
- Antenatal care
- Clinical trials
- Proficiency in:
- Basic computer applications
- Smartphone-based data tools
- Strong communication skills in:
- English
- Hindi
- Ability to work effectively in a multidisciplinary team
Desirable Skills
- Knowledge of Serious Adverse Event (SAE) reporting
- Experience in:
- Antenatal clinics
- Obstetric wards
- Neonatal wards
- Familiarity with:
- Informed consent procedures
- Verbal autopsy processes
Salary Details
- Salary: As per organizational norms
- Estimated Range: ₹30,000 – ₹45,000 per month (based on experience and qualification)
Why Apply for This Clinical Research Coordinator Role?
- Work on a prestigious ICMR-funded clinical research study
- Gain hands-on experience in maternal and neonatal clinical research
- Exposure to hospital-based clinical trial coordination
- Strengthen expertise in clinical documentation, adverse event reporting, and participant management
- Enhance career prospects in clinical research organizations (CROs), public health research, and regulatory roles
This opportunity is particularly suitable for professionals seeking growth in clinical trial management, maternal health research, and hospital-based research coordination.
Application Process
Interested candidates may:
📧 Email their updated CV to: careers@sas.org.in
🌐 Visit the official website: www.sas.org.in
