Clinical Scientist

Key Responsibilities: Assist the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studies Support medical monitoring activities, adjudication, imaging data reconciliation, and preparation of study meeting materials Review clinical study data and assist with identification and resolution of data discrepancies and queries Support protocol deviation review and management Review patient data, including adverse events, laboratory results, endpoints, and other clinical information Support one or multiple clinical studies depending on study needs May lead a study or workstream with limited scope, such as survival follow-up Interact with internal and external stakeholders, including study sites and committees, to support clinical study objectives

Qualifications: Degree in Life Sciences required (BS/BA/MS/PhD)Minimum of 2 years of pharmaceutical and/or clinical drug development experience within the last 5 years Experience may come from pharmaceutical/biopharmaceutical companies, CROs, hospitals, research sites, clinical trial units, or SMOsExperience reviewing and resolving study-related data issues, including queries and medical record/data review Ability to identify data discrepancies requiring clarification with clinical study sites Experience reviewing patient data and resolving discrepancies involving adverse events, laboratory results, endpoints, and safety data preferred Therapeutic-area experience required for Oncology positions; indication-specific experience preferred Strong written and verbal communication skills Proficiency with Microsoft Outlook, Word, Excel, and Power Point; One Note experience preferred