Clinical Research Coordinator

About the role

The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Director of Research and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols and regulating agency policies.

Responsibilities

• Follow protocol-specific requirements to successfully carry out the study
• Code, evaluate, or interpret collected study data
• Document and maintain required records necessary for study activities per local, state, and FDA GCP requirements
• Maintain professional communication with investigators, sponsors, and study personnel
• Willing to travel to various Urology San Antonio offices
• Must be flexible and adaptable to a changing environment with our growing research department
• Auxiliary function: Assist with identifying eligible patients for studies requiring case and healthy control subjects

Qualifications

• High attention to detail and strong organizational skills
• Excellent written and verbal communication skills
• Ability to work well independently
• Maintain confidentiality
• Experience with Microsoft Office Suite (Outlook, Word, Excel, PowerPoint)
• Clinical research certification a plus but not required
• Experience managing operations (coordinating/scheduling patient visits)
• Possess strong skills for multitasking, meeting competing deadlines, prioritizing and supporting PIs for multiple projects
• Research: 3-5 years

Requirements

• Current BLS
• Three or more years of recent Clinical Research experience with human participants
• Prior experience in a similar-sized facility and comparable services provided
• Experience and knowledge of the purpose and use of medication in the treatment of cancer

Benefits

Not specified

Pay

Not specified

Schedule

Not specified