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CareMother by Doto Health

Clinical Research Associate

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  • Posted 11 days ago
  • Over 50 applicants

Job Description

Job Title: Research Associate (Clinical Research)

Location: On-site, Pune AFMC

Organization: Dt Health | CareMother Incubated by IITB

On a Direct payroll of IIT Bombay

Salary : 20k per month

About Us: Dt Health (CareMother) is redefining women's healthcare with smart, tech-enabled solutions that improve access and outcomes. Our AI-powered tools support the full journey from pregnancy to newborn care, with a focus on early detection, high-risk pregnancy management, labor monitoring, and the impact of climate change on maternal health. We empower healthcare providers with data-driven tools to deliver better, safer care anytime, anywhere.

Role Summary: We are hiring a Research Associate to support a maternal health study at AFMC, Pune. This role involves clinical coordination, data collection, and observing how our monitoring technology is used in real settings.

Key Responsibilities:

Project management and Operations:

Anchor the on-site contact for all study activities at AFMC, Pune.

Establish and maintain strong working relationships with all project collaborators. Monitor project progress and address any operational challenges

Travel to meet stakeholders and facilitate smooth project execution, as needed Observe how clinicians use the device and record usability feedback. Work with the central team to analyze patterns and system performance. Study Design and Data Management:

Assist in study design, ensure alignment with research objectives.

Collect, evaluate, and validate data as per the clinical study protocols. Ensure data integrity and structure data appropriately for analysis.

Conduct preliminary data analysis to support research findings and project insights. Summarise and report study outcomes with attention to detail and accuracy. Ensure adherence to ethical standards and guidelines throughout the project. Maintain meticulous records and documentation of research findings. Ensure compliance with ethical and regulatory standards.

Reporting:

Maintain daily logs, timelines, and handle any study-related queries on-site. Prepare interim and final documentation including case summaries and findings. Share weekly/monthly reports and contribute to study documentation.

Qualifications:

Bachelor's or Masters degree in Medical, Biosciences, Biomedical, or a related field. Experience of work in a hospital settings and research coordination preferred Familiarity with data tools (Excel, SPSS, etc.).

Strong communication skills to work with clinical and technical teams. Willingness to travel.

Compensation: The role offers a monthly remuneration of 20,000 per month.

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Job ID: 134390195