Clinical Research Coordinator

The Clinical Research Coordinator will work closely with the Clinical Research Site Manager and is the primary contact for the study participants. The CRC will also work with the Study Doctor to ensure the safety and well-being of the study participant is protected.

Duties

• Obtaining informed consent per ICH/GCP and site SOPs.
• Pre-screening and collecting data from potential study participants.
• Scheduling, coordinating/completing study visits.
• Obtaining study participant vital statistics (including height, weight, BMI, pulse, respiratory rate, blood pressure, etc.), ECGs, spirometry or other procedures applicable per study protocol.
• Dispensing/collecting study medication and providing accurate Investigational Product accountability.
• Collecting subject laboratory specimens according to protocol.
• Completing case report forms (CRFs) and other patient tracking information (either electronic or manual) accurately and on a timely basis as assigned.
• Responding to any study visit data queries.
• Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.
• Other clinical research-related duties as assigned.
• This position requires flexibility, excellent organizational/communication skills and attention to detail.

Requirements

• 1 year experience as a Clinical Research Coodinator
• Reliable transportation to travel from site to site

Job Type: Full-time

Expected hours: 40 per week

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Application Question(s):

• How many years of experience do you have as a Clinical Research Coordinator?

Work Location: In person