Life Science Research Analyst

Cleartrip

Nagercoil, Chennai District

On-site

INR 900,000 - 1,300,000

Full time

3 days ago
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Job summary

Cleartrip is seeking a Life Science Research Analyst with ~4 years of experience to lead end-to-end SLR, TLR and meta-analysis support, delivering accurate, traceable results for pharmaceutical and health clients.

You will validate AI-assisted outputs, apply PRISMA, prepare evidence tables and reports, and contribute to quality checks, version control, and client-ready Word and PDF deliverables, with regular project meetings.

Qualifications

  • 4 years of experience in SLR, TLR and meta-analysis support.
  • Experience with AI-assisted review workflows across evidence streams.
  • Experience in data extraction and evidence synthesis with source-level traceability.

Responsibilities

  • Execute SLR and TLR tasks end to end: literature searches, deduplication, title/abstract screening, full-text screening, data extraction and evidence synthesis.
  • Support protocol development, research questions, eligibility criteria and search strategies, including repeat searches and comparison of search outputs against reference sets.
  • Extract structured data with source-level traceability (quotes and page references) using standardized templates, including data from tables and figures.
  • Validate AI-generated screening and extraction outputs, including table and figure parsing, against source documents and human-reviewed results, and document discrepancies.
  • Conduct risk of bias and quality assessments using tools suited to the study type (human observational, animal and mechanistic studies).
  • Support meta-analysis, including preparing data for quantitative synthesis and interpreting outputs.
  • Apply PRISMA and accepted evidence synthesis methods throughout.
  • Prepare evidence tables, summaries, reports and presentations, and produce accessible Word and PDF deliverables.
  • Maintain version control and respond to reviewer comments with documented change logs.
  • Contribute to quality checks and peer review of project outputs.
  • Take part in regular project status meetings and keep trackers up to date.

Skills

Literature reviews
Data extraction
Meta-analysis support
PRISMA
Quality assessment
Evidence synthesis
Screening

Job description

We are seeking a Life Science Research Analyst with about 4 years of experience in systematic literature reviews (SLR), targeted literature reviews (TLR) and meta-analysis support. You will execute review projects under the guidance of a project lead, from search and screening through reporting. You will work with AI-assisted review workflows across human, animal and mechanistic evidence streams, with a focus on accuracy, traceability and timely delivery for pharmaceutical, biotechnology, medical device and public health clients.

  • Execute SLR and TLR tasks end to end: literature searches, deduplication, title/abstract screening, full-text screening, data extraction and evidence synthesis.
  • Support protocol development, research questions, eligibility criteria and search strategies, including repeat searches and comparison of search outputs against reference sets.
  • Extract structured data with source-level traceability (quotes and page references) using standardized templates, including data from tables and figures.
  • Validate AI-generated screening and extraction outputs, including table and figure parsing, against source documents and human-reviewed results, and document discrepancies.
  • Conduct risk of bias and quality assessments using tools suited to the study type (human observational, animal and mechanistic studies).
  • Support meta-analysis, including preparing data for quantitative synthesis and interpreting outputs.
  • Apply PRISMA and accepted evidence synthesis methods throughout.
  • Prepare evidence tables, summaries, reports and presentations, and produce accessible Word and PDF deliverables.
  • Maintain version control and respond to reviewer comments with documented change logs.
  • Contribute to quality checks and peer review of project outputs.
  • Take part in regular project status meetings and keep trackers up to date.
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