Sr. Manager, Clinical Research Scientist

Position Summary:The Senior Manager, Clinical Research Scientist assists in designing, executing, and reporting Phase 1-3 clinical oncology trials. The role supports the medical monitor with key tasks related to trial design, conduct, monitoring, analysis, and reporting.Performance Objectives:Collaborate with team members (Medical Monitors, Project Managers, Clinical Operations, Data Management, Biostatistics, PV, PK, Biomarkers, Medical Writing) to deliver high-quality trial results.Use scientific expertise to create essential clinical documents (study protocols, CSRs, investigator brochures, DSUR, NDA/MAA registration documents, publications).Review and summarize clinical data to ensure study quality and protocol compliance.Stay updated on clinical development knowledge and apply it to study design and summaries.Inform the Sr. Medical Director about trial status and provide risk assessments.Perform other duties as required. Travel up to 25%.Education/Certification Requirements:Preferred: Master's degree in pharmaceutical or related medical science.Knowledge, Skills, and Abilities:3-5 years of drug development experience in the pharmaceutical industry.At least 2 years in oncology with exposure to clinical development (reviewing data quality, protocols, CSRs, investigator brochures, DSUR, NDA/MAA documents, publications).Ability to critically review and interpret clinical data.EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.To find out more about Real, please visit