Clinical Research Coordinator - 237654 - Medix : Job Details

Role: Clinical Research Coordinator (part time)

Location: Onsite

Therapeutic Area: Dermatology

Employment Type: Position is a contract, project based support role - current contract duration is estimated to be 3-6 months, possibility for extension

Schedule/ Shift:

• Part time, 24 hours a week
• Weekly schedule is TBD, open to reviewing candidates' preferences

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
• Collects, verifies, organizes and records clinical information and data in electronic data capture systems EDC.
• Abstracts data from necessary sources to complete the EDC and resolve queries.
• Performs the following data related activities: EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding

Minimum Education and Experience Qualification Requirements:

• Minimum 1 year experience with clinical trial coordination required
• Minimum 1 year experience with participant recruitment (screening over the phone, processing Media referrals, scheduling/appointment Reminders, retrieving medical records)
• Experience with Modernized Med EMR highly preferred