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7 days ago
Requirements and responsibilities
About The RoleWhat if your expertise in clinical research methodology could directly influence the quality and integrity of medical science? We're looking for Clinical Trial Research Scientists to critically evaluate clinical study protocols, trial designs, and study outcomes — helping ensure that the science behind new treatments meets the highest standards of methodological rigor.This is a fully remote, flexible contract role built for experienced professionals statistics, or pharmaceutical science who want meaningful, high-impact work on their own terms.What You'll DoReview and evaluate clinical trial protocols, identifying methodological strengths, gaps, and risksAnalyze endpoints, inclusion/exclusion criteria, randomization strategies, and study controls for scientific soundnessInterpret trial results and produce clear, accurate summaries of safety and efficacy findingsValidate statistical analysis plans for completeness, accuracy, and regulatory alignmentIdentify operational or scientific risks in trial execution before they become problemsSupport recurring evaluations of clinical documentation and study outputs across multiple projectsMust-HaveWho You AreHands-on experience statistics, pharmaceutical science, or a closely related fieldStrong working knowledge of trial methodology, GCP guidelines, and regulatory standards (FDA, EMA, or equivalent)Proven ability to interpret complex trial data and communicate findings clearly in written formDetail-oriented, methodical, and capable of working independently with minimal oversightNice To HaveExperience across Phase I–IV clinical trialsFamiliarity with specific therapeutic areas (oncology, cardiology, rare disease, etc.)Background ulatory affairs, or clinical data managementExposure to adaptive trial designs or Bayesian statistical approachesWhy Join UsWork on high-quality, scientifically meaningful projects that matterFully remote and flexible — work when and where it suits youFreelance autonomy with the structure of consistent, task-based assignmentsApply your expertise across a diverse range of trials and therapeutic areasPotential for ongoing work and contract extension as new projects launch