Clinical Research Coordinator (CRC) & Clinical Research Associate (CRA)
About Us
We are a health-tech company developing AI-powered digital auscultation technology to improve the early detection of cardiovascular diseases. Our innovative device, AyuSynk, records high-quality heart and lung sounds to assist clinicians in identifying abnormal cardiac conditions.
Following the successful completion of our pilot clinical study at a leading tertiary care hospital in Mumbai, we are expanding to a multicenter clinical study across four hospitals in India. The study aims to build a comprehensive heart sound database covering congenital heart disease (CHD) and other structural cardiac abnormalities to support AI model development and clinical validation.
We are looking for a highly motivated Clinical Research Coordinator (CRC) & Clinical Research Associate (CRA) who can coordinate the multicenter study while also managing clinical research activities at our Bengaluru study site.
Role Overview
This is a hybrid role combining the responsibilities of a Clinical Research Coordinator (CRC) and an on-site Clinical Research Associate (CRA).
As the CRC, you will coordinate study execution across multiple participating hospitals, ensuring smooth communication with Principal Investigators (PIs), ethics committees, and internal research teams.
As the CRA for the Bengaluru site, you will be responsible for day-to-day study operations, including participant recruitment, informed consent, heart sound data collection using the AyuSynk device, source documentation, data quality, and ensuring protocol compliance.
Key Responsibilities
Clinical Research Coordination (CRC)
● Coordinate multicenter clinical research activities across all participating hospitals.
● Serve as the primary liaison between Principal Investigators, Co-Investigators, ethics committees, and internal teams.
● Track study timelines, recruitment targets, milestones, and site performance.
● Schedule investigator meetings and regular study review calls.
● Coordinate study start-up activities, including site initiation and training.
● Ensure timely communication across all study sites.
● Support publication-related documentation and study reporting.
Bengaluru Site Clinical Research Associate (CRA)
● Conduct day-to-day study activities at the Bengaluru study site.
● Screen and recruit eligible participants according to the approved study protocol.
● Explain the study and obtain informed consent from participants.
● Collect high-quality heart and lung sound recordings using the iUsync device.
● Capture clinical data and complete Case Report Forms (CRFs) accurately.
● Maintain source documents and ensure complete study documentation.
● Resolve data queries in collaboration with investigators.
● Ensure adherence to study protocol, GCP guidelines, and regulatory requirements.
● Report protocol deviations, adverse events, and documentation issues promptly.
● Coordinate participant follow-up visits when required.
Qualifications
● Bachelor's or Master's degree in Life Sciences, Clinical Research, Pharmacy, Nursing, Biotechnology, Biomedical Sciences, or related fields.
● MBBS/BDS/BAMS/BHMS candidates are welcome to apply.
Pay: ₹25,000.00 - ₹35,000.00 per month
Work Location: In person
