Role OverviewWorks under the supervision of the Administrative Director of the CNCT and the Principal Investigator to provide assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; maintaining and updating data generated by the study, all IRB submissions such as application, amendments, annual reviews and adverse events, and communicating with national and international research collaborators.
What You Will Do
Assists with clinical research studies as per study guidelines and protocols; screen for eligibility, recruit and evaluate potential study patients; collects data and maintains the patient information database for several studies; interacts with patients/subjects regarding the studies, including patient education, procedural instruction, and follow-up.
Why It Might Be a Fit
Requires ability to work more independently and as a team member; computer literacy, analytical skills, and ability to resolve technical problems; ability to interpret the acceptability of data results; working knowledge of data management programs.
Requirements
- Bachelor's Degree required
- Related post-bachelor's degree research experience 1-2 years required
- Ability to work more independently and as a team member
- Computer literacy, analytical skills, and ability to resolve technical problems
- Ability to interpret the acceptability of data results
- Working knowledge of data management programs
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses as applicable
- Recognition programs designed to celebrate your contributions and support your professional growth
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