Job Description

Role : Clinical Research Coordinator

Location : Onsite - Miami, FL 33176

• Relocation candidates will NOT be considered for this position

Therapeutic Area : Asthma

Employment Type : Position is a contract, project based support role - current contract duration is estimated to be 2-4 months, possibility for extension

Schedule/ Shift:

• 30 hours a week, M-F
• Site is open as early as 7:30 AM for scheduling, but ideal work schedule would be 9-3pm M-F with some flexibility that if there is a need for them to come in earlier to help with patient screening etc or to handle calls.

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, Medical Record Retrieval, Community Outreach/Referral Physician Networking

Minimum Education and Experience Qualification Requirements:

• Candidates MUST be bilingual (fluent) in Spanish
• Minimum 1 year experience with clinical trial coordination required
• Minimum 1 year experience with participant screening and recruitment required
• Experience / knowledge related to Asthma preferred
• Experience with RealTime CTMS preferred

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