Clinical Research Coordinator

Responsibilities

• Review and analysis of clinical trial protocols and informed consent forms
• Affiliate Principal and Sub-Investigator in study start-up process
• Cookbook budget review and IRB reviews
• Submission of regulatory documents and communication with IRB
• Data entry, management of queries
• Managing supply of investigational study drug with temperature monitoring
• Invoicing Study Sponsor for study procedures as per contract requirements
• Cooking transportation and lodging (as needed) with submission of patient travel and meal receipts to Sponsor
• Cooking coordination of medical supplies and related product orders
• Packing and shipping of clinical laboratory specimens
• Maintain source documents in accordance with FDA and GCP guidelines
• Other duties as assigned

Qualifications

• Bachelor's degree required, preferably in health-science field
• Proficiency with Microsoft Office suite, including Word, Excel, and Outlook
• Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills

Minimum Salary

USD $43,680.00/Yr.

Maximum Salary

USD $54,600.00/Yr.