Adverse Events, Clinical Monitoring, Clinical Research, Clinical Trial, Detail Oriented, Documentation, FDA (Food and Drug Administration), Hospital, Informed Consent, Interpersonal Skills, Medical Records, Neurology, Project Tracking, Statistics
- Participates in the design, administration and monitoring of clinical trials.
- Responsibilities: Plans, organizes, performs and monitors daily project protocols.
- Collects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports.
- Reports and assists with the management of protocol deviations, adverse events and other project-related issues
- Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.
- Understanding of the Food and Drug Administration (FDA) rules is beneficial.
- Positions duties are clerical/administrative verses medical.
EDUCATION/EXPERIENCE REQUIRED: -
- High School diploma equivalency with 2 years of cumulative experience
- OR
- Associate degree/Technical degree
- OR
- 4 years of applicable cumulative job specific experience required.
Preferred skills;
- Bachelor's degree, experience with statistical analysis, attention to detail, adaptability, dependability, communication and interpersonal skills are preferred
- Critical thinking skills required.
Additional Information
- Organization: Henry Ford Providence Hospitals
- Department: HFPSH Research Neurology
- Shift: Day Job
- Union Code: Not Applicable