Project Research Scientist -II (Medical) - ICMR ENABLE 2

Stjohns

Bengaluru

Hybrid

INR 900,000 - 1,200,000

Part time

14 days+

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Qualifications

  • Two to three years' experience in a recognized institute/hospital.
  • MBBS /BVSc /BDS with MPH / PhD.
  • MBBS /BVSc /BDS + Post Graduate Degree, including the Integrated PG Degrees.
  • Preferred Language: Good Communication in English

Responsibilities

  • Involved in selection of sites and training.
  • Regulatory approvals.
  • Development of study tools
  • Quality assessment
  • Site contract, and communications with steering committee members
  • DSMB & sites.
  • Overall coordination.
  • Data management.
  • Statistical analysis and training of regional coordinator.

Skills

Good communication in English

Education

MBBS / BVSc / BDS with three years' experience
MBBS / BVSc / BDS with MPH / PhD
MBBS / BVSc / BDS + Post Graduate Degree

Job description

Home / Careers / Project Research Scientist -II (Medical) - ICMR ENABLE 2

Project Research Scientist -II (Medical) - ICMR ENABLE 2

Posted on: 12 Sep 2026

Employment Type: Contract

Experience: Two to three years' experience in a recognized institute/hospital

Job Summary:

ENABLE 2 is a hybrid type-2 implementation trial evaluating the effectiveness and scalability of an integrated, multi-level cardiovascular care model for vulnerable populations beyond healthcare settings

The project aims to strengthen cardiovascular disease prevention and care by engaging vulnerable and underserved communities and integrating community and health-system approaches. Community participation is central to the project, with local stakeholders and community members involved in delivering and supporting the intervention to reach the unreached. The study will assess health outcomes and implementation factors, including reach, adoption, implementation, and sustainability, to generate evidence for scaling up integrated cardiovascular care models in India.

Vacancy: One

Key Responsibilities:
  • Involved in selection of sites and training.
  • Regulatory approvals.
  • Development of study tools
  • Quality assessment
  • Site contract, and communications with steering committee members
  • DSMB & sites.
  • Overall coordination.
  • Data management.
  • Statistical analysis and training of regional coordinator.
Eligibility Criteria:

Preferred Qualifications:

  • MBBS /BVSc /BDS with three years' experience /
  • MBBS /BVSc /BDS with MPH / PhD
  • MBBS /BVSc /BDS + Post Graduate Degree, including the Integrated PG Degrees.

Preferred Language:Good Communication in English

Good Knowledge in Clinical data collection, including interviews/surveys

Experience of working in Public Health/Medical Research Projects

Age Limit: 40 Years

Tentative Date of Joining :1st October 2026

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