Ayur.AI Recruitment – Clinical Research Associate, Chennai

Ayur.AI is hiring a Clinical Research Associate for its clinical research team in Chennai, Tamil Nadu. This opportunity is suitable for candidates with a background in Life Sciences, Medicine, Nursing, Public Health, or related healthcare disciplines. The role involves coordinating clinical trial participants, managing study data, supporting biospecimen logistics, and maintaining research documentation in line with Good Clinical Practice (GCP) and Institutional Review Board (IRB) protocols. Candidates with 1–2 years of experience in clinical research or healthcare are encouraged to review the opportunity.

Company Overview

Ayur.AI focuses on personalized health and wellness through AI-powered Ayurveda solutions. Its platform offers personalized programs addressing metabolic health, gut health, and women’s health.

The company is also developing Integrative Diabetes Centers that combine Ayurveda, modern science, technology, and personalized health insights to address diabetes.

Job Details

Job Role & Responsibilities

The selected candidate will support the daily operations of longitudinal clinical trials involving Continuous Glucose Monitoring (CGM), laboratory testing, gut microbiome analysis, and remote physician consultations.

Participant Coordination

• Schedule and follow up on appointments for CGM setup, laboratory tests, stool sample collection, and virtual consultations.

• Provide participants with clear instructions on app usage and study-related test procedures.

Data Collection & Management

• Monitor and collect data from wearable CGM devices and study-related applications.

• Enter and validate participant data in study databases and Case Report Forms (CRFs) within the required timelines.

• Identify and report data inconsistencies or protocol deviations to the study coordinator or Principal Investigator (PI).

Communication & Support

• Coordinate communication between participants, clinical laboratories, logistics partners, physicians, and the internal research team.

• Maintain regular and empathetic communication with participants to encourage study adherence and address concerns.

• Coordinate specimen shipment and tracking with third-party laboratories.

Documentation & Compliance

• Maintain accurate participant records in accordance with Good Clinical Practice (GCP) and IRB protocols.

• Maintain participant information sheets, informed consent forms, and data-tracking documents.

Eligibility & Qualifications

Candidates should have a bachelor’s degree in a health-related discipline, such as Life Sciences, Medicine, Nursing, Public Health, or a similar field.

Relevant courses may include B.Sc. Life Sciences, M.Sc. Life Sciences, B.Pharm, M.Pharm, Pharm.D, B.Sc. Nursing, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Microbiology, M.Sc. Microbiology, or Public Health qualifications, where relevant to the employer’s health-related qualification requirement.

Experience Requirements

• Experience in a clinical research or healthcare setting is preferred.

• Relevant internships may also be considered.

• Knowledge of laboratory logistics and biospecimen handling is beneficial.

• Familiarity with Continuous Glucose Monitoring (CGM) devices and mobile health-tracking tools is an advantage.

Required Skills

• Proficiency in spreadsheets, including Microsoft Excel or Google Sheets.

• Familiarity with electronic data capture (EDC) platforms or research data management systems.

• Strong organizational skills and attention to detail.

• Excellent verbal and written communication skills.

• Ability to work independently, manage time efficiently, and handle multiple tasks.

• Ability to communicate with patients remotely and explain technical procedures in simple language.

• Empathetic, proactive, and collaborative approach to participant support.

 

How to Apply

Interested candidates can review the job listing and apply through LinkedIn.

Apply here: Clinical Research Associate – Ayur.AI

Applicants should review the official listing for the latest application status and any additional employer requirements.

Job Summary