Clinical Scientist
$80,000–$130,000 year
On-site · Princeton, New Jersey, United States or Redmond, Washington, United States
Job Summary
Clinical Scientist to join the clinical development team. Responsibilities include monitoring, reviewing, and summarizing safety and efficacy data in ongoing studies; translating the clinical protocol into operational deliverables (Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines); responding to study questions from sites/vendors; conducting literature searches and reviews to support new trial design and regulatory documents; preparing scientific material; contributing to SOPs and templates; and participating in cross-functional meetings with clinical operations, safety, regulatory, biostatistics, and data management. Qualifications include a life sciences or health-related degree, 3-4 years of industry experience (clinical research preferred), oncology therapeutic area experience, data cleaning/visualization and basic statistics (Excel mandatory, R optional), knowledge of ICH and GCP, ability to analyze and socialize data to internal/external stakeholders, strong communication and strategic capabilities, and the ability to work independently and meet timelines. Compensation ranges from $80,000 to $130,000 annually with a comprehensive benefits package; Equal Opportunity Employer.
Required Qualifications
- Degree in life sciences or health-related field
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