Analysis Skills, Clinical Research, Clinical Trial, Clinical Trial Management, Data Collection, Detail Oriented, Establish Priorities, Interpersonal Skills, Medical Records, Medical Terminology, Microsoft Office, Organizational Skills, Presentation/Verbal Skills, Problem Solving Skills, Project/Program Management, Team Player, Time Management, Training/Teaching, Writing Skills
Under the supervision of a Clinical Research Supervisor, Project Manager, or Principal Investigator (PI), the Clinical Research Coordinator (CRC) will perform entry-level duties related to the support and coordination of clinical studies and may receive training and development to prepare and advance to the next level within the series.
Required Qualifications:
- HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training
- Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team
- Attention to detail
- Proficiency with Microsoft Office Suite and REDCap
- Excellent analytical and problem-solving skills
- Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects
- Ability to establish cooperative working relationships with patients, co-workers, & physicians
Preferred Qualifications:
- Demonstrated proficiency with medical terminology.
- Experience working with patients or study subjects.
- Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.