Clinical Research Coordinator II — Lead High-Quality Trials

DM Clinical Research; Humble (TX); On-site; USD 60,000 - 75,000; Full time

Job summary

A clinical research organization is seeking a Clinical Research Coordinator II in Humble, TX to oversee the execution of clinical trials. The successful candidate will ensure quality research is conducted in compliance with protocols and regulations. Responsibilities include participant visits, data management, and regulatory compliance. A high school diploma is required, with a bachelor's degree preferred and at least 2 years of CRC experience. Energetic and detail-oriented individuals will thrive in this role.

Qualifications

• At least 2 years of experience as a Clinical Research Coordinator.
• Preferred experience coordinating industry-sponsored vaccines.
• ACRP or equivalent certification preferred.

Responsibilities

• Ensure compliance with sponsor protocol, FDA regulations, and ICH/GCP guidelines.
• Conduct study subject visits and document procedures.
• Complete data entry and query resolution in a timely manner.
• Maintain knowledge of current FDA regulations and protocols.
• Oversight of reporting all adverse events as per company guidelines.

Skills

Detail-oriented

Multi-tasking

Energetic

Goals-driven

Education

High School Diploma or equivalent

Bachelor's degree

Foreign Medical Graduates

Tools

ICH-GCP Certification

IATA Certification

Job description

A clinical research organization is seeking a Clinical Research Coordinator II in Humble, TX to oversee the execution of clinical trials. The successful candidate will ensure quality research is conducted in compliance with protocols and regulations. Responsibilities include participant visits, data management, and regulatory compliance. A high school diploma is required, with a bachelor's degree preferred and at least 2 years of CRC experience. Energetic and detail-oriented individuals will thrive in this role.