Subject Matter Expert (SME) - Generative AI - Orthopedics

Cactus Communications; Vancouver; Remote; CAD 120,000 - 180,000; Part time

Benefits offered by this job

Flexible, asynchronous engagement

Project-based (no fixed hours)

Job summary

Cactus Communications is seeking accomplished physician-researchers to serve as Subject Matter Experts in GenAI for medical research. The SME will help design GenAI-enabled products and ensure scientific rigor across evidence generation and dissemination.

You will collaborate with cross‑functional teams—clinical researchers, data scientists, engineers, and product managers—to translate clinical needs into testable workflows, conduct methodological reviews, and validate GenAI outputs.

Qualifications

• MD degree with specialization in Internal Medicine and active U.S. clinical license required
• Advanced academic or research training such as PhD/MPH/MS desirable
• Peer‑reviewed publications as first/senior author in high-impact journals
• Hands-on experience with RCTs, systematic reviews, or meta-analyses
• PI experience desirable
• Familiarity with PubMed/Embase/Cochrane Library and data extraction tools

Responsibilities

• Guide product/workflow design for clinical research including systematic reviews, RCTs, and meta-analyses
• Evaluate and validate GenAI outputs for scientific accuracy and rigor
• Integrate clinical and biomedical data sources into AI-enabled tools and agents
• Collaborate with product managers, data scientists, UX designers, and developers to define test cases and workflows
• Provide clinical review during GenAI model selection, tuning, testing, and refinement

Skills

GenAI in medicine

NLP in healthcare

Clinical research

Literature review

Education

MD (Internal Medicine)

Board-certified Internal Medicine

PhD/MPH/MS in Clinical Research/Epidemiology

Tools

PubMed

Embase

Cochrane Library

Job description

Freelance Subject Matter Experts (GenAI in Medical Research)

We are seeking accomplished physician-researchers to serve as Subject Matter Experts (SME) in the field of Generative AI for medical research. The SME will be instrumental in supporting the development and validation of Generative AI (GenAI) products designed to advance medical research and evidence synthesis. They will collaborate closely with cross-functional teams to design GenAI-enabled products and workflow solutions that aim to improve the quality, speed, and reliability of medical evidence generation, translation, and dissemination. They will serve as a scientific bridge, connecting medical researchers, GenAI engineers, data scientists, UX designers, software developers, and product managers.

Ideal candidates will be active physicians with hands‑on experience conducting, supervising, or participating in clinical research studies, randomized controlled trials (RCTs), systematic reviews, or meta‑analyses. They should also have a strong publication record as first or senior authors in peer‑reviewed, high‑impact journals. A thorough understanding of research methodology and publication ethics is highly desirable.

Job Responsibilities

Medical and Research Expertise

• Provide expert guidance in product and workflow design to support a wide spectrum of clinical research, including systematic reviews, narrative and scoping reviews, randomized controlled trials (RCTs), and qualitative studies.
• Evaluate and validate GenAI outputs to ensure scientific accuracy, methodological rigor, and compliance with established standards and frameworks such as CONSORT, PRISMA, and GRADE.
• Facilitate the integration of clinical and biomedical data sources into AI‑enabled tools and agents, with an emphasis on journal content.

Product and Technology Collaboration

• Work collaboratively with product managers, GenAI data scientists, UX designers, and software developers to define clinically relevant test cases for GenAI agents and translate clinical workflows into AI‑assisted research capabilities, including protocol formulation, literature screening, structured data extraction, quality appraisal, and evidence synthesis.
• Translate complex clinical and research requirements into actionable design specifications and define evaluation metrics for GenAI agent accuracy, bias, and reliability in research and publication settings.
• Provide clinical review and feedback throughout GenAI model selection, tuning, testing, and refinement processes.

Thought Partnership

• Serve as a clinical thought leader who informs agentic product development within the medical and research domains.
• Support teams in interpreting clinical data, research methodologies, and publication standards.
• Represent the organization in selected customer engagements.

Qualifications and prerequisites

Education and Clinical Training

• An MD degree with specialization in Internal Medicine, board certification in this specialty, and an active U.S. clinical license in good standing are required.
• Additionally, an advanced academic or research training is highly desirable, such as a PhD, MPH, or MS in Clinical Research, Biomedical Informatics, or Epidemiology.
• Demonstrated record of peer‑reviewed publications as a first or senior author in high‑impact journals.
• Hands‑on experience in conducting or supervising randomized controlled trials (RCTs), systematic reviews, or meta‑analyses.
• Principal Investigator experience is desirable.
• Familiarity with medical databases such as PubMed, Embase, ClinicalTrials.gov, and the Cochrane Library, as well as with modern data extraction or curation tools.

Preferred Technical and Domain Competencies

• Working knowledge of Generative AI, natural language processing (NLP), and machine learning as applied to medical research.
• Strong analytical and critical appraisal skills, particularly in evaluating GenAI‑assisted outputs.
• Excellent communication skills and ability to collaborate effectively with clinicians, data scientists, engineers, and product managers.

Benefits of the role:

• Flexible, asynchronous engagement
• Project-based (no fixed hours)