CRC II Research Coordinator

Benefits : 401(k)

Competitive salary

Health insurance

Opportunity for advancement

Training & development

Job Summary

We are seeking a motivated and detail-oriented Research Coordinator to join our team. The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies.

Responsibilities

• Provide clinical research support to investigators to prepare for and execute assigned research studies, including :
• Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
• Attend all relevant study meetings;
• Collect and submit regulatory / ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
• Recruit and screen patients for clinical trials and maintain subject screening logs;
• Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
• Design and maintain source documentation based on protocol requirements;
• Schedule and execute study visits and perform study procedures;
• Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;
• Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
• Monitor subject safety and report adverse reactions to appropriate medical personnel;
• Correspond with research subjects and troubleshoot study-related questions or issues;
• Participate in meetings to confirm daily study tasks are assigned to team members and are executed to the expected standards;
• Assist with study data quality checking and query resolution.

Qualifications

Must have 3 years as a coordinator

Spanish Speaking / Bilingual preferred