Responsibilities for Clinical Research Coordinator

• Responsible for ensuring study is compliance with local and federal laws and regulations
• Recruits and screens potential study participants and performs intake assessments
• Creates and/or maintains all documents and records related to the study
• Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
• Manages the inventory of equipment and supplies related to the study and orders more as needed
• Attends meetings, events and seminars in order to promote the study
• Collects specimens and inputs data and patient information into electronic systems
• Creates reports on each study, including notes on protocols, workload, data collection, and more

Qualifications for Clinical Research Coordinator

• 2+ years previous experience working in a clinical setting (preferred)
• Excellent written and verbal communication skills
• Superior organizational and time management skills
• Capable of working independently with minimal supervision and also as part of a team
• Skilled with standard computer programs
• Understanding of medical terminology as well as standard clinical procedures and protocols
• Proficient in venipuncture, ECG and vital signs

Job Type: Full-time

Pay: $38,000.00 - $48,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Employee discount
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Education:

• High school or equivalent (Required)

Experience:

• Venipuncture: 1 year (Required)
• Clinical research: 1 year (Required)

Work Location: One location

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