Home/Job List/Clnical Research Coordinator cum Registry Lead (Ludhiana)
Christian Medical College & Hospital

Clnical Research Coordinator cum Registry Lead (Ludhiana)

Christian Medical College & Hospital

Ludhiana, Punjab, India
Full-Time
Posted 24 days ago

Opens the application on shine.com

Job Description & Responsibilities

About the Role

The Neuromuscular Center of Excellence India's first accredited Duchenne Center (World Duchenne Organization) is seeking a Pharm D graduate to serve as Clinical Research Coordinator and Registry Lead. This role combines your pharmacology and clinical trial training with hands-on ownership of the center's patient registry and research operations, positioning you at the center of the program's move toward gene therapy and drug development trial-readiness.

Key Responsibilities

Clinical Research Coordination

  • Coordinate patient recruitment, scheduling, and follow-up for research studies and future clinical trials
  • Support protocol development and drug-related trial documentation, drawing on your pharmacology background
  • Assist with pharmacovigilance monitoring and adverse event documentation as trial activity grows
  • Prepare and maintain ethics committee (IEC) submissions and CDSCO-related regulatory documentation

Registry & Data Management

  • Own and maintain the center's patient/research registry (DMD, SMA, and other rare NMD patients)
  • Ensure data quality, completeness, and audit-readiness across all registry entries
  • Support biostatistics and data analysis for grant reporting (ICMR) and scientific submissions
  • Help prepare abstracts, posters (e.g., World Muscle Society), and manuscript drafts

Program Support

  • Coordinate research-related logistics with the multidisciplinary clinical team
  • Support materials and documentation for global partnerships and the upcoming TREAT-NMD masterclass

Light coordination with front-office/administrative staff on research-related scheduling

Requirements

  • Pharm D degree (mandatory)
  • Strong understanding of pharmacology, clinical trial methodology, and GCP principles
  • Detail-oriented with strong data management skills (Excel, REDCap, or similar)
  • Comfortable working directly with physicians, patients, and families
  • Interest in rare disease research and long-term growth opportunities in clinical trials/drug .

Required Skills

GCPExcel

Job Details

Employment TypeFull-Time
Work ModeOn-Site
Experience0 – 0 years
Positions1

Posted by

N/A

Posted on:

5 Oct 2026

About Christian Medical College & Hospital

More open roles

Browse all jobs →