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Systematic Review Consultant Jobs (NOW HIRING)

Senior Consultant, VAP

New York, NY ยท On-site

$118K - $177K/yr

EVAP Senior Consultants have unique opportunities to manage project workstreams and provide ... General understanding of systematic review methods, clinical research design, and applicable ...

Senior Consultant, VAP

New York, NY ยท On-site

$118K - $177K/yr

EVAP Senior Consultants have unique opportunities to manage project workstreams and provide ... General understanding of systematic review methods, clinical research design, and applicable ...

Senior Consultant, VAP

New York, NY ยท On-site

$118K - $177K/yr

EVAP Senior Consultants have unique opportunities to manage project workstreams and provide ... General understanding of systematic review methods, clinical research design, and applicable ...

Senior Consultant, VAP

New York, NY ยท On-site

$118K - $177K/yr

EVAP Senior Consultants have unique opportunities to manage project workstreams and provide ... General understanding of systematic review methods, clinical research design, and applicable ...

Showing results 21-40

Systematic Review Consultant information

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$34

$65

How much do systematic review consultant jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for systematic review consultant in the United States is $34.22, according to ZipRecruiter salary data. Most workers in this role earn between $26.92 and $38.46 per hour, depending on experience, location, and employer.

What is a systematic review consultant?

Systematic Review Consultants are professionals who specialize in guiding and supporting research teams through the systematic review process. They help design review protocols, develop search strategies, manage literature screening, extract data, assess study quality, and synthesize findings. These consultants ensure that systematic reviews are conducted according to rigorous and transparent standards, making results reliable and reproducible. Their expertise is often sought by academic researchers, healthcare organizations, and policy makers to produce high-quality evidence syntheses.

How does a systematic review consultant typically collaborate with subject matter experts during a project?

A Systematic Review Consultant often works closely with subject matter experts (SMEs) to ensure the review protocol is methodologically sound and addresses relevant research questions. Consultants facilitate initial meetings to align on objectives, clarify inclusion and exclusion criteria, and refine search strategies. Throughout the project, they coordinate regular check-ins to discuss findings, resolve uncertainties in data extraction, and interpret nuanced results, ensuring the final report is both accurate and meaningful to the field. This collaborative approach not only enhances the quality of the review but also fosters professional development through interdisciplinary teamwork.

What are the key skills and qualifications needed to thrive as a systematic review consultant, and why are they important?

To thrive as a Systematic Review Consultant, you need expertise in literature search strategies, data extraction, critical appraisal, and a strong background in research methodology, often supported by an advanced degree in health sciences or a related field. Familiarity with reference management software (e.g., EndNote), systematic review management tools (e.g., Covidence, RevMan), and guidelines such as PRISMA is typically required. Attention to detail, strong analytical skills, and effective communication help consultants manage complex data and collaborate with interdisciplinary teams. These skills ensure the delivery of rigorous, transparent, and high-quality evidence syntheses that inform policy and practice.

What are popular job titles related to Systematic Review Consultant jobs?

For Systematic Review Consultant jobs, the most frequently searched job titles are:

Sr. Consultant, Value, Access, and Pricing

Manhattan, NY โ€ข On-site

Trinity Partners, LLC
Real Estateย โ€ขย 51 - 200 employees

$110K - $140K/yr

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Position Responsibilities
  • Lead analysis of primary and secondary data to generate meaningful value, access, pricing insights and recommendations for our clients (biopharmaceutical / pharmaceutical companies) across US payer and stakeholder types, including both qualitative (e.g., IDIs, focus groups, ad-boards) and quantitative project work.
  • Support team members by coordinating and guiding the work of more junior staff members and effectively communicating as a partner to project managers and leadership.
  • Create and present clientโ€‘ready materials, including research materials, interim deliverables, and final project reports.
  • Provide thought leadership in evidence strategy, value, market access and pricing in both clientโ€‘ and nonโ€‘clientโ€‘related activities (e.g., external conferences).
  • Train and mentor more junior staff during projects, in internal training efforts, and through formal / informal mentorship.
  • Support business development activities (e.g., proposal writing) as training for future role as a BD lead.
  • Support the growth of the EVAP function through involvement in internal initiatives focused on consultantโ€™s professional development, training, and resources.
Position Requirements
  • Bachelorโ€™s degree with high academic achievement; major in health sciences, Economics, or HEOR, and demonstrated interest in life sciences is a plus.
  • 3โ€“4 years as a top performer within a topโ€‘tier biopharmaceutical / pharmaceutical strategy consulting firm serving industryโ€‘leading clients on USโ€‘related business questions.
  • Deep knowledge of the US healthcare system and pricing dynamics, with demonstrated understanding of different payer / provider types (and related access nuances), as well as trends within the US industry.
  • Working knowledge of essential and advanced consulting methodologies, tools, and techniques.
  • Excellent analytical skills and numeric capability.
  • Strong oral and written communication skills in English language.
  • Ability to use PubMed / Medline, Google Scholar, research platforms to source reimbursement data.
  • Proficiency in MS Office Suite (Microsoft Word, PowerPoint, and Outlook).
  • General understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials.
  • High attention to detail with superior organizational and timeโ€‘management skills.
  • Strong team player, ability to work with crossโ€‘functional staff.
  • Ability to work under the pressure of deadlines and manage multiple priorities.
Compensation and Benefits

A reasonable estimate of the current range is $110,000โ€“$140,000. In addition to your base salary, you will also be eligible for an annual discretionary performance bonus.

Equal Opportunity Employer

Trinity Life Sciences is an equal opportunities employer and welcomes applications from all qualified individuals.

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