Clinical Research Coordinator - Houston

We have an exciting opportunity for a Clinical Research Coordinator to join an innovative team while creating the next generation of clinical trials.
This company provides rapid, scalable solutions so that physicians can participate in clinical trials and offer state of the art care options to their patients. They also help underserved communities access the best possible care by reaching broad and diverse trial participant and patient populations.
If you are an energetic, independent, and compassionate Clinical Research Coordinator (CRC) and looking for a career that will be rewarding in so many ways, then we would love to hear from you. The position is based in Houston, TX. The successful candidate will possess a willingness and desire to work independently without significant supervision.

• Manages the inventory of equipment and supplies related to the study.
• Facilitate regulatory start up-documentation and filings, including central IRB submissions.
• Responsible for ensuring study compliance with local and federal laws and regulations.
• Processes specimens and inputs data and patient information into electronic systems.
• Schedule and coordinate protocol-specified study visits.
• Acts as a point of reference for study participants by answering questions and keeping them informed on the study programs.
• Creates and/or maintains all documents and records related to the study.
• Recruits and prescreens potential study participants and may perform intake assessments.
• Creates reports and trackers on each study, including notes on protocols, workload data collection and more.

Requirements

• Spanish Speaking
• 2-3 years of working in clinical trials

Benefits

• Insurance: Medical, Dental and Vision options, eligible after 60 days of employment
• Car Allowance: Mileage reimbursement (IRS max of $.585/mile for study-related local travel)
• PTO: 3 weeks (15 days) per year
• 401k Plan: 100% Vested, 6% Company match, eligible after 90 days of employment