Systematic Reviewer, HEOR
Location: India (Remote)
Company: Global HEOR Consultancy
Position type: Full-time
Compensation: Competitive salary, commensurate with experience and seniority.
Company Overview
We are a global HEOR and HTA consultancy focused on developing evidence across the pharmaceutical product lifecycle.
We support pharmaceutical and biotechnology clients with evidence generation, evidence synthesis, indirect treatment comparisons, economic and value demonstration, HTA strategy, and reimbursement-focused deliverables. Our work is grounded in the belief that evidence must withstand scrutiny — methodologically, analytically, and contextually.
Why this role is important
We are seeking an experienced Systematic Reviewer, HEOR to join our growing consultancy team in India.
This role is suited to someone with a strong foundation in systematic literature review methods who can contribute to the delivery of rigorous, high-quality evidence synthesis projects across clinical, economic, humanistic, epidemiologic, and HTA evidence areas.
The successful candidate will work closely with senior reviewers, statisticians, health economists, analysts, and company Directors to support projects for global pharmaceutical and biotechnology clients, with a focus on generating evidence for HTA, reimbursement, and scientific communication.
What success looks likeIn 3 months
- Build a strong understanding of our project workflows, quality standards, templates, and client expectations.
- Contribute independently to screening, data extraction, quality assessment, and evidence synthesis activities.
- Support the development of SLR protocols, search strategies, extraction frameworks, and technical reports.
- Deliver accurate, well-documented work within agreed timelines.
In 6 months
- Independently manage key SLR workstreams with limited oversight.
- Contribute to protocol development, search strategy review, screening decisions, data extraction planning, quality assessment, synthesis, and reporting.
- Support junior team members and contribute to quality-control activities.
- Participate in project meetings and communicate clearly on progress, risks, and evidence gaps.
In 12 months
- Lead defined components of complex SLR projects from protocol through final reporting.
- Provide methodological input into review design and evidence synthesis approaches.
- Take increasing responsibility for reviewing junior team members' work.
- Contribute to the continuous improvement of internal SLR processes, templates, and quality standards.
What you’ll be doing
- Conduct systematic literature reviews across clinical, economic, humanistic, epidemiologic, and HTA evidence areas.
- Contribute to protocol development, eligibility criteria, search strategy review, screening, data extraction, quality assessment, evidence synthesis, and reporting.
- Support targeted literature reviews, evidence gap assessments, HTA reviews, and related evidence synthesis projects.
- Develop high-quality deliverables, including SLR protocols and reports, evidence tables, HTA evidence summaries, manuscripts, abstracts, posters, and payer-facing materials.
- Apply established review methodologies and reporting standards to ensure work is rigorous, transparent, reproducible, and fit for purpose.
- Perform quality control and peer review of screening, data extraction, and written deliverables.
- Work across multiple concurrent projects while managing timelines, priorities, and documentation.
- Collaborate with senior reviewers, statisticians, health economists, and other project team members.
- Support and mentor junior reviewers and analysts where appropriate.
What you’ll bring
- Master’s degree in health economics, epidemiology, public health, pharmacy, medicine, outcomes research, life sciences, or a closely related discipline.
- 2–3+ years of relevant experience in systematic literature reviews, evidence synthesis, HEOR, HTA, or market access, ideally within a consultancy environment.
- Hands-on experience conducting SLRs across one or more evidence areas, including clinical efficacy and safety, economic evaluations, cost and resource use, utilities, health-related quality of life, epidemiology, or HTA.
- Experience with key stages of the SLR process, including screening, data extraction, quality assessment, evidence synthesis, and technical reporting.
- Strong scientific writing, critical appraisal, analytical, and communication skills.
- High attention to detail and commitment to methodological quality.
- Ability to manage multiple tasks and deadlines across concurrent projects.
- Strong proficiency in Microsoft Word, Excel, and PowerPoint.
Would love for you to have
- Experience developing SLR protocols and contributing to search strategy development or peer review.
- Experience with HTA requirements or evidence expectations in Canada, the UK, or Europe / EU Joint Clinical Assessment.
- Familiarity with PRISMA, GRADE, Cochrane methods, NICE methods guidance, CDA-AMC requirements, or EU JCA evidence requirements.
- Experience with systematic review software such as DistillerSR, Covidence, EPPI-Reviewer, or similar platforms.
- Experience contributing to manuscripts, conference abstracts, posters, or other scientific publications.
- Experience reviewing or mentoring junior team members.
What you’ll get
- Opportunity to join a growing global HEOR and HTA consultancy.
- Remote role based in India, with close collaboration across international teams.
- Exposure to complex and diverse evidence synthesis projects across multiple therapeutic areas.
- Opportunity to work with pharmaceutical and biotechnology clients across multiple jurisdictions.
- Structured opportunities to develop deeper expertise in SLR methodology, HTA, evidence synthesis, and indirect treatment comparisons.
- Supportive, collaborative environment with opportunities for professional growth and increasing project responsibility.
How to apply
Interested candidates should submit a CV and brief cover letter outlining their relevant experience in systematic literature reviews, evidence synthesis, HEOR, HTA-focused deliverables, and scientific writing.
Benefits:
- Paid sick time
- Paid time off
- Provident Fund
- Work from home
Work Location: Remote
