Principal/Senior Clinical Data Scientist

原始資料於 2026-11-04T15:06:58.463335+00:00 查閱；內容可能已更新，請查看原始職位。

Qualifications:
Minimum Required:
Bachelor’s degree or equivalent combination of education/experience in science or health-related discipline with proficiency in medical terminology
Minimum of 8 years of clinical research experience or proven competencies for this position
Minimum of 3 years Oncology experience, must have been within the past 1.5 years
Minimum of 1 year of leadership experience
Other Required:
High Proficiency with Microsoft Office Products (Outlook, Word, Excel, PowerPoint, Teams, OneNote).
Excellent organization skills, attention to high quality and detail, and a customer service demeanor, communication and interpersonal skills to effectively interface with others in a team setting and written and oral including presentations of data, issues, trends, escalations, etc..
Professional use of the English language; both written and oral
Ability to occasionally travel domestically and internationally including overnight stays (up to approximately 25%).
Preferred:
Medical related degree, RN, OCN, RPH, PharmD, etc.
Strongly preferred: Experience with Electronic Data Capture (EDC) systems
Database build experience
On-site experience (nurse, study coordinator, etc.), monitoring, &/or data review experience
Experience with data visualization platform(s)/software(s) as data review tools
Experience in phase I, II & III studies and global studies
Skills & Competencies:
Demonstrates highly advanced knowledge in oncology & medical terminology with ability to apply knowledge to clinical trial data including the application of disease assessment criteria, standards of care, grading criteria, etc. in a clinical research setting
Desire to continually learn and keep up to date on medical and indication-specific standards of care with the ability to self-research and educate, results oriented, exhibiting self-motivation and reliably, with the ability to work remotely while independently lead, support and inspire excellence.
Demonstrates scientific curiosity and an investigative mindset, with the ability to identify atypical data patterns, formulate hypotheses, from a scientific and clinical focus, and drive appropriate follow-up actions.
Working knowledge of FDA & ICH-GCP, relevant SOPs & regulatory guidance with a well-rounded knowledge of the entire clinical trial process and working understanding of clinical research functional departments.
Ability to independently manage the Clinical Science operational function in a global, cross-functional environment with awareness of appropriate escalation.
Excellent time management, negotiation, critical thinking, decision making, listening, analytical & conflict management skills with the ability to strategically plan & apply effective risk management.
Demonstrates ability to adjust to multiple demands & shifting priorities.
Demonstrates ability to mentor, coach, and develop junior team members while fostering a collaborative learning environment.
Ability to apply financial management skills at the functional area project level.
Excellent presentation, verbal & written communications skill
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