We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports





Your profile
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 3 years of experience as a Clinical Research Associate & On-Site Monitoring
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Oncology/Immunology TA is mandatory
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced workplace.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

📌 Clinical Research Associate (Mumbai)
🏢 Trigent Software
📍 Mumbai