Bangalore
The ICMR-funded Secure Ultrasound (Secure US) Project is an innovative initiative focused on developing and validating a screenless ultrasound device aimed at addressing critical challenges in maternal healthcare. This project is driven by the need to combat female feticide and overcome the shortage of skilled ultrasound operators in rural Indian health centers. This project is undertaken by Division of Medical Informatics at St. John s Research Institute, which makes use of innovative tools and techniques to drive health systems research and healthcare innovation for improving healthcare outcomes with meaningful use of data.
Key Responsibilities:
- Assist in the implementation, and management of research activities related to the SecureUS Project.
- Conduct data collection, management, and assist in preliminary analysis for the evaluation of the screenless ultrasound device.
- Work closely with other project staff to coordinate field validation and usability studies.
- Assist in the development of survey instruments, interview guides, and research tools for stakeholder consultations, including hospital administrators and healthcare workers.
- Maintain detailed project documentation, including research protocols, consent forms, lab notes, project activities and ethics committee submissions.
- Travel to project sites for field validation and stakeholder studies.
- Organize and participate in stakeholder meetings, workshops, and training sessions for research staff and healthcare workers.
- Monitor project timelines, data quality, and regulatory compliance under the guidance of the supervising officer.
- Support field teams in troubleshooting data collection challenges and ensure adherence to ethical research practices.
- Analyze qualitative and quantitative data using statistical software and visualization tools.
- Conduct literature reviews and assist in drafting research papers, reports, and presentations.
- Assist in grant writing and proposal development for securing additional funding.
Eligibility Criteria:
Preferred Qualifications:
- BDS, AYUSH or equivalent degree in a relevant medical or clinical field.
- Additional qualifications such as MPH, PhD, or specialization in Epidemiology, Public Health or Clinical Research are desirable.
Experience :
- Minimum 1-3 years of experience in clinical research, medical device validation, or public health studies.
- Experience in working on medical device research, maternal and child health, or community-based healthcare projects is preferred.
- Proficiency in data analysis software (SPSS, R, STATA, NVivo, or similar).
- Experience in qualitative and quantitative research methodologies, data management, and literature review.
- Prior experience in manuscript writing and research grant applications is desirable.
- Familiarity with Good Clinical Practice (GCP) guidelines.
- Experience in collaborating with national and international research organizations is an advantage.
Age Limit: 35 Years
Preferred Language: English Kannada Telugu, Tamil and Hindi (Optional)
Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
1-3 years96
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Job Description
Download ResumeBangalore
The ICMR-funded Secure Ultrasound (Secure US) Project is an innovative initiative focused on developing and validating a screenless ultrasound device aimed at addressing critical challenges in maternal healthcare. This project is driven by the need to combat female feticide and overcome the shortage of skilled ultrasound operators in rural Indian health centers. This project is undertaken by Division of Medical Informatics at St. John s Research Institute, which makes use of innovative tools and techniques to drive health systems research and healthcare innovation for improving healthcare outcomes with meaningful use of data.
Key Responsibilities:
- Assist in the implementation, and management of research activities related to the SecureUS Project.
- Conduct data collection, management, and assist in preliminary analysis for the evaluation of the screenless ultrasound device.
- Work closely with other project staff to coordinate field validation and usability studies.
- Assist in the development of survey instruments, interview guides, and research tools for stakeholder consultations, including hospital administrators and healthcare workers.
- Maintain detailed project documentation, including research protocols, consent forms, lab notes, project activities and ethics committee submissions.
- Travel to project sites for field validation and stakeholder studies.
- Organize and participate in stakeholder meetings, workshops, and training sessions for research staff and healthcare workers.
- Monitor project timelines, data quality, and regulatory compliance under the guidance of the supervising officer.
- Support field teams in troubleshooting data collection challenges and ensure adherence to ethical research practices.
- Analyze qualitative and quantitative data using statistical software and visualization tools.
- Conduct literature reviews and assist in drafting research papers, reports, and presentations.
- Assist in grant writing and proposal development for securing additional funding.
Eligibility Criteria:
Preferred Qualifications:
- BDS, AYUSH or equivalent degree in a relevant medical or clinical field.
- Additional qualifications such as MPH, PhD, or specialization in Epidemiology, Public Health or Clinical Research are desirable.
Experience :
- Minimum 1-3 years of experience in clinical research, medical device validation, or public health studies.
- Experience in working on medical device research, maternal and child health, or community-based healthcare projects is preferred.
- Proficiency in data analysis software (SPSS, R, STATA, NVivo, or similar).
- Experience in qualitative and quantitative research methodologies, data management, and literature review.
- Prior experience in manuscript writing and research grant applications is desirable.
- Familiarity with Good Clinical Practice (GCP) guidelines.
- Experience in collaborating with national and international research organizations is an advantage.
Age Limit: 35 Years
Preferred Language: English Kannada Telugu, Tamil and Hindi (Optional)
Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.