Clinical Scientist
New
S
Sarah Cannon Research InstituteOncology Research
United StatesFull-TimeMiddle
SalaryCompetitive compensation package. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.
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Job Details
- Experience
- 2+ years
- Required Skills
- Data Analysis
Requirements
- Bachelor’s Degree (4-year program) required.
- Minimum 2+ years of experience analyzing data and science in clinical research and/or laboratory-based research or within the pharmaceutical or CRO environment.
- Prior work experience in a highly-detailed role such as nursing or scientific research.
- Prior work experience in a collaborative environment taking initiatives when needed such as process improvement.
- Experience in oncology clinical research and/or oncology-focused laboratory-based research preferred.
- Familiarity with medical data review preferred.
- Knowledge of ICH-GCP and regulatory requirements.
Responsibilities
- Serve as the scientific point of contact for the study team on both industry-sponsored and investigator-initiated trials.
- Collaborate with medical writing during the development of clinical study protocols and attend protocol development meetings.
- Perform medical and scientific review of clinical study protocols, informed consent forms, investigator brochures, case report forms, clinical study reports, TFL shells, TFLs, and other study documentations and publications.
- Perform medical data review and assessments of safety and efficacy data.
- Scientifically review clinical research data including patient demographics, medical and disease history, concomitant medications, laboratory values, adverse events, disease response verification, and overall review to enhance data quality.
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