Clinical Trial Research Scientist

* Review clinical trial protocols and identify methodological strengths, gaps, and risks * Analyze endpoints, inclusion/exclusion criteria, study controls, and design choices * Interpret trial results and produce clear, well-reasoned summaries of safety and efficacy findings * Validate statistical analysis plans for completeness, accuracy, and regulatory alignment * Identify operational or scientific risks in trial execution and documentation * Support recurring evaluations of clinical study outputs with consistency and precision * Work independently and asynchronously — on your own schedule

Who You Are

Must-Have: * Solid experience in clinical research, biostatistics, pharmaceutical science, or a related field * Strong working knowledge of trial methodology, regulatory standards, and good clinical practice * Ability to interpret complex trial data and communicate findings clearly and concisely * Detail-oriented and systematic — you catch what others miss * Self-motivated and comfortable delivering high-quality work independently

Nice to Have: * Hands-on experience across Phase I–IV clinical trials * Familiarity with specific therapeutic areas (oncology, CNS, cardiovascular, etc.) * Background in regulatory submissions, medical writing, or protocol development * Experience reviewing or contributing to statistical analysis plans

Why Join Us

* Apply your expertise to meaningful scientific work with real-world impact * Fully remote and flexible — work when and where it suits you * Freelance autonomy with the structure of consistent, task-based engagements * Work on diverse trial types and therapeutic areas that keep the work intellectually engaging * Potential for ongoing assignments and contract extension as new projects launch