Clinical Research Coordinator

Overview
We are seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to join our team and support DHA. In this role, you will manage and oversee the daily operations of various research studies, which may include case series, cross-sectional studies, systematic reviews, case-control studies, cohort studies, and randomized clinical trials.

The specific responsibilities of the CRC are defined by the Principal Investigator (PI), with whom the CRC works closely. The CRC plays a key role in ensuring that studies are conducted in compliance with the study protocol, applicable regulations, Good Clinical Practice (GCP), and Institutional Review Board (IRB) requirements.

In addition to administrative tasks, the CRC may serve as a liaison for the clinical site, ensure study staff are appropriately trained according to protocol, recruit and/or register participants, maintain adherence to study procedures, and collect or review study data prior to database entry. The CRC collaborates with research teams, sponsors, and monitors to support efficient study progress and timely completion

Responsibilities

• Communicates with investigators and study team to manage the day-to-day activities of the study including problem solving, communication and protocol management
• Schedules and facilitates study meetings
• Manages the IRB process
• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility
• Monitors study performance to ensure that all processes, protocols & procedures are quality controlled and functioning up to standards
• Develops implements & administers budgets, grant & administrative procedures
• Coordinates and collects data in accordance with the study protocol
• Maintains study documentation and study files to include consent forms, source documents, case report forms
• Assures timely completion of Case Report Forms
• Provides administrative support to team members and client as requested to ensure success of the program
• Assists investigators with the development and implementation of recruitment strategies in accordance with IRB approvals.
• Establishes and organizes study files, study specific source documentation and other materials.
• Maintains Regulatory Binder
• Coordinates and meets study timelines

Experience

• Must have a minimum of five years of experience in a research clinical setting
• Must have a minimum of two years of experience in project management
• Must have DOD and or federal contracting experience

Education/Certification

• Bachelor’s degree or higher in a scientific discipline
• Institutional Review Board (IRB) Collaborative Institutional Training Initiative (CITI Program); must recertify every three years
• Good Clinical Practice (GPC) certification within two months of hire
• Project Management Professional (PMP) certification (preferred)

Join our team as a Clinical Research Coordinator and contribute to advancing medical knowledge through innovative research!

Job Types: Full-time, Contract

Pay: From $55,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Work Location: In person

Salary : $55,000