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 cutting-edge 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 quick-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