What are the responsibilities and job description for the Clinical Research Coordinator - 240640 position at Medix™?
Role: Clinical Research Coordinator
Location: Onsite - Canton, MI 48187
- Relocation candidates will NOT be considered for this position
- Role is 100% onsite, there is no opportunity for hybrid or remote work at this time
Therapeutic Area: Dermatology
Employment Type: Position is a contract, project based support role - current contract duration is estimated to be 2 months, possibility for extension
Schedule/ Shift:
- Part Time, 24 hours a week
- M-F during daytime business hours (open to reviewing candidates' preferred work schedules)
Responsibilities/ Job Duties:
This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices.
Responsibilities -
- May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO
- Contractor will focus support on recruitment activities including Chart Review, Phone Screening, Scheduling/Appointment Reminders,
- Contractor will assist with EDC Data Entry
- Contractor will also provide support with Source Document Storage, Regulatory Support
Minimum Education and Experience Qualification Requirements:
- Minimum 1 year experience with clinical trial coordination required
- Minimum 1 year experience with participant screening and recruitment required
- Minimum 1 year experience with EDC Data entry and query resolution
- Minimum 1 year experience with Source Document Storage, and providing Regulatory Support
- Experience / knowledge related to immunology preferred
