Clinical Research Coordinator
- Ability to effectively present information and respond to questions from physicians, patients, fellow research staff, and office staff.
- High level of organization and self-motivated to manage multiple projects simultaneously.
- Good organizational and interpersonal skills
- Ability to understand and follow detailed instructions
- Strong time management capability and ability to work efficiently on multiple tasks.
- Skill in developing and maintaining relationships, and communicate calmly and clearly with patients and medical staff.
- Strong time management and ability to work efficiently on all tasks.
- Ability to use tact, discretion, and sound judgment when dealing with confidential information.
- Good interpersonal skills and ability to work as part of a team is essential.
- Exceptional attention to detail and accuracy.
- Bachelor's degree in health science or related field or equivalency
- Minimum of three years of professional clinical research experience
- Certification with Association of Clinical Research Professionals, or with Society of Clinical Research Associates, or intention of obtaining same within 1 year of employment.
- Oversight and coordinate for all sponsored research at Jordan Young Institute
- Budget management including invoice and payments for the research foundation from research sponsors
- Study coordinator for sponsored trials including patient screening, consenting, enrolling and managing throughout the study protocol
- Maintenance of IRB CITI training course
- Basic understanding of medical terminology/research
- Experience with clinical trial contract negotiation and budget negotiation a plus
- Proficient with MS Office (Word, Excel), email, internet, data entry
- Ability to transpose information from clinical document to computerized database
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