Clinical Scientist, Hematology
Bristol Myers Squibb
Google Cloud Platform
Clinical Research Coordinator
Duke Careers
full-time
Posted on:
Location: North Carolina • 🇺🇸 United States
Visit company websiteSalary
💰 $59,829 - $99,960 per year
Job Level
JuniorMid-Level
About the role
- Responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking, and provision to research participants.
- Serves as the primary liaison with sponsors, Investigational Drug Service (IDS), and other parties as necessary.
- Follows protocol schema for randomization and blinding and unbinding.
- Prepares for and provides support for study monitoring and audit visits, including support for the reviewer.
- Addresses and corrects findings.
- Conducts activities for study visits in compliance with the protocol.
- Conducts and documents consent for participants for all types of studies, including those that are complex in nature and require any orders in Maestro Care.
- Ensures accuracy and completeness of data for all studies, including those that are complex in nature.
- Recognizes data quality trends and escalates as appropriate.
- May develop tools for, and train others in, data quality assurance procedures.
- Collects appropriate information to determine whether the study teams participation in a specific trial is feasible.
- May make feasibility recommendations.
Requirements
- Completion of an Associate’s Degree
- A minimum of two years of relevant research experience.
- A Bachelor’s degree may substitute for two years required experience.
- Can easily use computing software and web-based applications (e.g., Microsoft Office products and internet browsers).
- Hybrid eligible. The position (exempt only) is partially remote, and the employee must reside in a Duke University-approved state.
