The CRA will collaborate closely with project managers, investigators, and cross-functional teams to maintain high-quality execution of clinical trials and support overall operational efficiency.

Qualifications
Robust understanding of clinical trial Protocols and the ability to interpret and apply protocol requirements in day-to-day site monitoring.
Experience working as Clinical Research Associates or in similar monitoring roles within clinical research environments.
Knowledge of Clinical Trials processes, including study start-up, conduct, monitoring, and close-out activities.
Solid background in Research and Clinical Operations, with familiarity in coordinating stakeholders and managing site-level activities.




Bachelor’s or Master’s degree in life sciences, pharmacy, nursing, or a related field.
Knowledge of Positive Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
Solid attention to detail, analytical skills, and ability to identify and resolve issues proactively.
Effective written and verbal communication skills, with the ability to work collaboratively across multicultural teams.
Proficiency in using clinical trial management systems, electronic data capture tools, and standard office software.

📌 Clinical Research Associate Delhi
🏢 Intrinseque Health
📍 Delhi