[Remote] Clinical Researcher

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a fast-growing AI Data Services company and subsidiary of SuperAnnotate, delivering training data for many of the world’s largest AI companies. They are seeking a Clinical Researcher Subject Matter Expert to evaluate AI-generated clinical research content and create expert research content, ensuring accuracy and reputed company in scientific problem-solving.

Responsibilities

• reputed company reputed company 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, reputed company, and contextual relevance
• Ensure Model reputed company: Test AI outputs for inaccuracies, misleading evidence interpretation, unsafe recommendations, and bias; validate reliability across use cases

Skills

• 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 reputed company)
• 5+ years of professional experience in clinical research (academia, hospitals, CROs, biopharma, public health research, or similar)
• Strong reputed company 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, reputed company bias)
• Exceptional attention to detail reputed company fact-checking; minimum reputed company English proficiency with strong scientific writing
• Reliable, self-directed, and reputed company to deliver consistent quality in an hourly, remote contractor workflow across time zones
• Familiarity with clinical trial operations concepts (protocols, deviations, AE/SAE logic, data quality, monitoring) and/or GCP principles is a plus
• Prior experience with AI data training/annotation, medical/scientific editorial QA, systematic reviews, or guideline work is strongly preferred

Benefits

• If reputed company, you will be among the first experts we reputed company out to reputed company relevant opportunities arise
• reputed company to future projects available through our expert network

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