Clinical Researcher

SME Careers; Metro Manila; Remote; PHP 3,461,000 - 5,192,000; Part time

Job summary

SME Careers is seeking a Clinical Researcher SME for an hourly remote contractor role. You will review AI-generated clinical research content and create expert research content, evaluating reasoning quality and problem-solving, while providing precise written feedback.

You will assess solutions for accuracy, safety, and adherence to the prompt, and fact-check medical claims. Responsibilities include developing AI training content, optimizing AI performance, and ensuring model integrity across

Qualifications

• Bachelor’s degree or higher in public health or related field.
• 5+ years of professional clinical research experience.
• Strong command of study design, endpoints, power analysis, and results interpretation.
• Excellent scientific writing and English proficiency (C1).

Responsibilities

• Develop AI training content with prompts and gold-standard answers.
• Evaluate and rank AI responses for correctness, rigor, clarity.
• Ensure model integrity by testing outputs for inaccuracies, bias, and unsafe recommendations.

Skills

Clinical research

Statistical reasoning

Evidence interpretation

Scientific writing

English C1

Remote work

Education

Bachelor’s degree or higher

Job description

In this hourly, remote contractor role, you will work as a Clinical Researcher Subject Matter Expert (SME) to review AI-generated clinical research and biomedical content and/or create expert research content, evaluating reasoning quality and step-by-step scientific problem-solving while providing precise written feedback. You will assess solutions for accuracy, clarity, safety, and adherence to the prompt; identify errors in study design, statistics, endpoint selection, bias/confounding, clinical trial methodology, and evidence interpretation; fact-check medical and scientific claims; write high-quality explanations and model solutions that demonstrate correct research reasoning; and rate and compare multiple responses based on correctness and reasoning quality. This role is with SME Careers, a fast-growing AI Data Services company and subsidiary of SuperAnnotate, delivering training data for many of the world’s largest AI companies and foundation-model labs. Your clinical research expertise directly helps improve the world’s premier AI models by making their evidence appraisal, trial interpretation, and research communication more accurate, reliable, and clearly explained.

Important

There is no immediate project for this role; however, if qualified, you will be among the first experts we reach out to when relevant opportunities arise. This will also provide you with access to future projects available through our expert network.

Key Responsibilities

• Develop AI Training Content: Create detailed prompts and gold-standard answers across clinical research methodology, interpretation, and scientific communication.
• Optimize AI Performance: Evaluate and rank AI responses to improve correctness, rigor, clarity, and contextual relevance.
• Ensure Model Integrity: Test AI outputs for inaccuracies, misleading evidence interpretation, unsafe recommendations, and bias; validate reliability across use cases.

Your Profile

• Bachelor’s degree (or higher) in a relevant field (e.g., Public Health/MPH, Epidemiology, Biostatistics, Clinical Research, Biomedical Sciences, PharmD, MD/DO, RN, or related).
• 5+ years of professional experience in clinical research (academia, hospitals, CROs, biopharma, public health research, or similar).
• Strong command of clinical research fundamentals: study design, endpoints, inclusion/exclusion criteria, power/sample size intuition, and interpretation of results.
• Comfortable evaluating statistical reasoning (effect sizes, confidence intervals, p-values, multiple comparisons, missing data, sensitivity analyses).
• Deep understanding of bias, confounding, and causality (randomization, blinding, selection bias, measurement bias, survivorship, collider bias).
• Familiarity with clinical trial operations concepts (protocols, deviations, AE/SAE logic, data quality, monitoring) and/or GCP principles is a plus.
• Exceptional attention to detail when fact-checking; minimum C1 English proficiency with strong scientific writing.
• Reliable, self-directed, and able to deliver consistent quality in an hourly, remote contractor workflow across time zones.
• Prior experience with AI data training/annotation, medical/scientific editorial QA, systematic reviews, or guideline work is strongly preferred.