CRA, Medical Writing, Pharmacist, Custodian, Investigational Quality Management & More

Roles & Responsibilities:

• Assist in execution of clinical trials as per protocol and SOPs
• Support subject screening, registration, and study documentation
• Maintain clinical trial data, logs, and regulatory records
• Ensure compliance with ICH-GCP and internal quality standards
• Support quality management, medical writing, or sample collection activities (role-dependent)

Qualification:

• B.Sc
• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)
• B.Sc Nursing / GNM
• Diploma in Medical Laboratory Technology (DMLT)

Experience:

• 0–3 years
• Freshers with relevant academic exposure can apply

Skills:

• Basic knowledge of clinical research processes
• Good documentation and communication skills
• Willingness to learn and work in a CRO environment
• Attention to detail and compliance orientation

Walk-in Details:

Walk-in Date: 21 January 2026

Interview Mode: Face-to-Face

Selection Process: HR Interview

About the Company:

Aizant Drug Research Solutions is a reputed Clinical Research Organization (CRO) providing end-to-end services in clinical trials, pharmacovigilance, medical writing, and quality management, supporting global pharmaceutical and biotech companies.