Role & responsibilities

Assist with site file maintenance, Investigator Site File organisation, and basic Case Report Form

(CRF) completion review for assigned studies

- Support patient recruitment coordination and screening log maintenance under CRA supervision
- Learn segment-specific documentation requirements across Pharma Regulatory, Medical Device,

and AYUSH/Nutraceutical studies

- Shadow senior CRAs on site initiation, monitoring, and close-out visits to build toward

independent site management

- Support routine data query resolution and follow-up documentation
- Assist with study-level administrative tasks, including courier tracking, supply management, and

meeting scheduling

- Maintain accurate records of training completion and site-specific requirements per study protocol

Required qualifications & experience

- M.Pharm / B.Pharm graduate, up to 2-3 years of relevant clinical research experience
- Exposure to site coordination and documentation practices, ideally across 4-5 studies (academic,

internship, or professional)

- Basic understanding of Positive Clinical Practice principles

📌 Clinical Trial Associate (New Delhi)
🏢 Auriga Research
📍 New Delhi