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

- Strong 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.
- Strong 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