Senior Clinical Scientist

Job Summary

Providing scientific and writing support for clinical strategy and trial development, the full-time Senior Clinical Scientist will focus on data analysis, clinical data dissemination, and collaboration with internal and external stakeholders in a remote setting.

Key Responsibilities

• Contribute to evidence development and clinical research strategies in collaboration with clinical science teams and advisory groups
• Develop study design options and clinical endpoints to facilitate decision-making and assess budgetary impacts
• Create data visualizations and coordinate submissions to scientific meetings while maintaining a library of relevant literature

Required Qualifications

• Bachelor's degree in Life Sciences, engineering, statistics, or related field; advanced degree (MS, PhD, MD) preferred
• Minimum of 12 years' experience in clinical research, particularly in the medical device industry and oncology clinical trials
• Experience in authoring and reviewing clinical documents with a working knowledge of GCP, ICH, and FDA regulations
• Proficiency with statistical software packages (e.g., SAS, R, SPSS) and strong analytical skills for data interpretation
• Excellent writing and presentation skills, with the ability to work independently on multiple projects