Remote Clinical Trial Scientist: Protocols & Stats

Alignerr Corp.; Seattle (WA); On-site; USD 96,000 - 152,000; Part time

Job summary

Alignerr Corp. seeks a Clinical Trial Research Scientist to critically evaluate study protocols, trial designs, and outcomes, ensuring methodological rigor across medical research programs.

The role is fully remote, flexible, contract-based, and suitable for seasoned professionals in clinical research, biostatistics, or pharmaceutical science who want meaningful, high-impact work on their own terms. You will review endpoints, inclusion criteria, randomization, and safety findings, and you will

Qualifications

• Hands-on experience in clinical research, biostatistics, pharmaceutical science, or a closely related field
• Strong 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 form
• Detail-oriented, methodical, and capable of working independently with minimal oversight

Responsibilities

• Review and evaluate clinical trial protocols, identifying methodological strengths, gaps, and risks
• Analyze endpoints, inclusion/exclusion criteria, randomization strategies, and study controls for scientific soundness
• Interpret trial results and produce clear, accurate summaries of safety and efficacy findings
• Validate statistical analysis plans for completeness, accuracy, and regulatory alignment
• Identify operational or scientific risks in trial execution before they become problems
• Support recurring evaluations of clinical documentation and study outputs across multiple projects

Job description

Alignerr Corp. seeks a Clinical Trial Research Scientist to critically evaluate study protocols, trial designs, and outcomes, ensuring methodological rigor across medical research programs.

The role is fully remote, flexible, contract-based, and suitable for seasoned professionals in clinical research, biostatistics, or pharmaceutical science who want meaningful, high-impact work on their own terms. You will review endpoints, inclusion criteria, randomization, and safety findings, and you will