Job Description

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

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