Role Overview
The Clinical Trial Research Scientist evaluates clinical study protocols, trial designs, endpoints, statistical plans, and study results. This role emphasizes methodological rigor, documentation clarity, and accurate interpretation of safety and efficacy outcomes.
What You’ll Do
– Review clinical trial protocols and identify methodological strengths or gaps
– Analyze endpoints, inclusion/exclusion criteria, and study controls
– Interpret trial results and summarize safety and efficacy findings
– Validate statistical analysis plans for completeness and accuracy
– Identify operational or scientific risks in trial execution
– Support recurring evaluations of clinical documentation and study outputs
What You Bring
Must-Have:
– Experience in clinical research, biostatistics, or pharmaceutical science
– Strong understanding of trial methodology and regulatory standards
– Ability to interpret trial data and communicate findings clearly
Nice-to-Have:
– Experience with Phase I–IV trials or specific therapeutic areas
$40 – $80 an hour
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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