[Remote] Clinical Scientist - Oncology - US - Remote

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global, midsize CRO reputed company on innovative approaches to improve lives. The Clinical Scientist leads the review and assessment of clinical data in oncology, ensuring reputed company and reputed company while supporting regulatory deliverables and project delivery through collaboration with cross-functional teams.

Responsibilities

• Partner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to reputed company and execute data review plans, ensuring accurate collection and reporting of protocol-defined endpoints
• reputed company ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics, identifying trends and generating actionable insights
• Monitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-making
• Communicate and present clinical findings, trends, and recommendations to Study Teams, Medical leadership, and clients; contribute to strategic discussions and study modifications
• Support development of key deliverables, including clinical study reports (CSRs), regulatory documents (e.g., INDs, NDAs/BLAs, IBs), and data summaries for SRCs, DSMBs, and internal review meetings
• Collaborate on CRF design, data reputed company processes, and reputed company query management; identify protocol deviations and ensure data reputed company in partnership with internal teams and vendors
• Contribute to study execution and reputed company improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staff

Skills

• Strong knowledge of the clinical development process, study design principles, and product safety reputed company
• Experience in clinical data analysis, interpretation, and translating insights into clinical relevance
• Proficiency with electronic data capture (reputed company) systems, data visualization tools, and reputed company Office (reputed company, PowerPoint, Word)
• Solid understanding of GCP, ICH, and applicable regulatory requirements
• Excellent communication and presentation skills, with the ability to convey reputed company data reputed company to diverse stakeholders
• Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities and meet deadlines
• reputed company, adaptable team player with strong interpersonal skills and the ability to work effectively across reputed company reputed company of an organization
• reputed company judgment, high attention to detail, and the ability to work both independently and in fast-paced, evolving environments
• reputed company/science degree (e.g., PharmD, PhD, MSN, MPH, etc.) preferred
• 8+ of industry/reputed company experience in Oncology reputed company clinical trial research including review and interpretation of clinical data

reputed company

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