Clinical Trial Associate

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 Good Clinical Practice principles