Clinical Research & Medical Intelligence Lead
Bengaluru, India · Full-time
- Posted 1mo ago
- From Visit Health’s careers page
- Location
- Bengaluru, India
- Type
- Full-time
- Experience
- 3+ years
- Department
- Healthcare
Opens the listing on getvisitapp.keka.com
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About the role
About the Role
We are looking for a Clinical Research & Medical Intelligence Lead to build and strengthen the clinical intelligence layer across Visit Health's healthcare products and services.
This is a research-oriented, clinically rigorous role for someone who can independently evaluate medical evidence, translate it into clinical frameworks and decision logic, and work closely with Product, Data, Engineering, and healthcare teams to operationalize it at scale.
The role will involve developing and validating clinical parameters, medical formulas, risk scores, thresholds, assessment frameworks, recommendation logic, and clinical protocols across Health Risk Assessments, Smart Health Reports, disease profiles, preventive health programs, and condition-management journeys.
The person will also play a key role in establishing clinical quality, governance, documentation, and research processes, with the opportunity to build and eventually lead the Clinical Research & Medical Intelligence function.
Location
Noida / Bangalore
Experience
3–7 years of relevant experience in one or more of the following:
- Clinical or Medical Research
- Medical / Scientific Writing
- Digital Health / Health-tech
- Preventive Healthcare
- Clinical Product Development
- Healthcare Consulting
- Clinical Quality or Governance
- Epidemiology / Public Health
- Evidence-based healthcare
Candidates with strong clinical research, analytical, and medical intelligence capabilities may also be considered even if their experience does not fit neatly into the above categories.
Mandatory Qualification
- MBBS
Preferred
- Experience in clinical research, medical writing, scientific research, or systematic literature review
- Strong understanding of clinical guidelines and evidence-based medicine
- Experience working with clinical protocols, risk assessment frameworks, or healthcare products
- Certification or additional qualification in Clinical Research, Epidemiology, Public Health, Digital Health, Health Informatics, or Healthcare Analytics
- Master's degree / MBA in Healthcare Management, Public Health, or a related field is an advantage
Key Responsibilities
1. Clinical Research & Evidence Validation
- Conduct structured medical and scientific research using peer-reviewed literature, clinical guidelines, and other credible evidence-based sources.
- Evaluate the quality, relevance, and applicability of clinical evidence.
- Build evidence summaries and recommendations to support healthcare products and clinical frameworks.
- Continuously review emerging clinical evidence and assess its relevance to existing products and protocols.
2. Clinical Framework & Risk Model Development
- Develop and validate clinical parameters, biomarkers, formulas, indices, scoring systems, thresholds, and risk-assessment methodologies.
- Define clinical interpretation and risk-stratification logic for different health conditions and patient profiles.
- Ensure that clinical frameworks are scientifically sound, internally consistent, and practical to implement at scale.
3. Health Risk Assessment & Medical Intelligence
- Develop and enhance clinical frameworks for Health Risk Assessments, Smart Health Reports, disease profiles, and condition-management journeys.
- Define interpretation logic, risk categories, recommendations, escalation criteria, and appropriate clinical next steps.
- Translate medical evidence into structured and actionable health insights for users.
4. Clinical Algorithms & Care Recommendations
- Develop evidence-based decision frameworks and algorithms for:
- Preventive care
- Health screening and diagnostics
- Specialist referrals
- Lifestyle interventions
- Health coaching
- Condition management
- Personalized care journeys
- Work with Product and Engineering teams to translate clinical logic into scalable product requirements and rules.
5. Medical & Scientific Writing
- Create and maintain clinical research documents, evidence summaries, protocols, guidelines, clinical content, and medical documentation.
- Convert complex clinical concepts into clear, structured, and actionable documentation for both clinical and non-clinical stakeholders.
- Build and maintain a structured clinical knowledge repository.
6. Clinical Quality, Governance & SOPs
- Contribute to the development of clinical quality standards and governance frameworks.
- Develop and maintain SOPs, documentation standards, clinical protocols, audit mechanisms, and quality-control processes.
- Support doctor evaluation frameworks and clinical quality reviews to ensure consistency across healthcare services.
- Identify gaps in clinical processes and recommend improvements.
7. Cross-Functional Product Collaboration
- Partner closely with Product, Data, Engineering, Doctors, Health Coaches, Diagnostics, and Operations teams.
- Translate clinical requirements into clear, implementable frameworks and product specifications.
- Review product features and healthcare journeys from a clinical accuracy, safety, and evidence perspective.
- Balance clinical rigor with usability, scalability, and real-world implementation.
8. Build the Clinical Research & Medical Intelligence Function
- Establish structured processes for clinical research, evidence review, validation, documentation, and governance.
- Build reusable clinical frameworks, repositories, templates, and review mechanisms.
- Take ownership of strengthening the Clinical Research & Medical Intelligence capability as the function scales.
- Over time, contribute to building the team, operating model, and standards for the function.
What We Are Looking For
- Strong foundation in clinical medicine and evidence-based healthcare.
- Demonstrated ability to independently research, interpret, and synthesize medical literature.
- Strong understanding of clinical guidelines, protocols, risk assessment, and clinical decision-making.
- Comfortable working with clinical parameters, biomarkers, formulas, indices, thresholds, and risk scores.
- Ability to translate complex medical knowledge into structured, practical, and scalable frameworks.
- Strong medical and scientific writing capability.
- High degree of scientific rigor and attention to detail.
- Strong analytical and problem-solving skills.
- Ability to challenge assumptions and validate clinical logic rather than relying solely on convention.
- Comfortable working with Product, Data, Engineering, and business stakeholders.
- Ability to operate independently and build processes in a fast-paced health-tech environment.
Key Skills
- Clinical & Medical Research
- Evidence-Based Medicine
- Literature Review & Evidence Synthesis
- Clinical Guidelines & Protocol Development
- Medical & Scientific Writing
- Clinical Algorithms & Decision Frameworks
- Risk Stratification & Risk Assessment
- Medical Formulas, Indices & Biomarker Interpretation
- Preventive Healthcare
- Disease Risk Assessment
- Digital Health / Health-tech
- Clinical Quality & Governance
- SOP & Process Development
- Healthcare Product Development
- Clinical Documentation & Knowledge Management
Skills they ask for
Pick one to see other roles that ask for it.
- Clinical research
- Evidence based medicine
- Literature review evidence synthesis
- Clinical guidelines protocol development
- Scientific writing
- Clinical algorithms decision frameworks
- Risk stratification risk assessment
- Medical formulas indices biomarker interpretation
- Preventive healthcare
- Risk assessment
- Digital health
- Clinical governance
- Process development
- Healthcare product development
- Clinical documentation knowledge management
About Visit Health
Health benefits and care access for employeesVisit Health provides health benefits for employers and insurers, including outpatient care, telehealth, mental health, wellness programs, and access to medical providers.
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