Job Description

Job Description

Job Description

Urology Associates Of Central California is currently looking for a Clinical Research Coordinator to join our team. The ideal candidate must be a self starter and be able to manage multiple projects, previous experience as a Research Coordinator and is familiar with the medical field. Two year of experience needed.

The Clinical Research Coordinator performs a variety of clinical study activities to assist the Principal Investigator in the conduct of a clinical study.

• Must be proficient in Microsoft Office Word and Excel
• Electronic health systems and data bases used in research environment
• willingness to demonstrate proficiency with in six months of hire
• Able to read, analyze and interpret information from professional journals, technical procedures, or governmental regulations.
• Coordinate protocol related research procedures, study visits, and follow up care
• report adverse events
• Phlebotomy experience preferred
• At least 2 years of clinical research coordinating experience
• Ability to adhere to IRB approved protocols
• Assist with screening participants for study and eligibility & enroll with accuracy in various databases.
• Assist with scheduling of subject appointments in accordance with the protocol and call subjects with study reminders.
• Understand protocol structure and how to interpret study requirements to assess study compliance and ensure quality control.
• complete simple to moderately complex data collection tasks and understand and follow proper documentation techniques.
• May help maintain study supplies, lab, kits, and reorder as needed.
• Prepares patients for office visits
• Ability to independently as well as in a team environment.
• Knowledge of GCP, federal state and local regulations, including HIPPA policies and procedures.
• Schedules study participant appointments and serves as the patient liaison and other participating physicians.
• works closely with participants in an integral way in the informed consent process by communicating clearly and openly with potential study patient about protocols open to enrollment.
• records adverse events
• Ensures that all materials for each trial protocol are available for subject enrollment.
• Support Clinical Research Coordinators and assist in maintaining good clinical practice standards in all study activities.
• Ensure accurate data collection and proper documentation if research activities following FDA, GCP, and study protocols.
• Prepare, process, label and store biological samples according to research protocols, ensuring timely shipping to central laboratories.
• Assist with screening participants for study eligibility and ensure accurate enrollment in research databases.
• Prepare, process, label and store biological samples according to research protocols, ensuring timely shipping to central laboratories.
• Assist physicians and nurses during patient visits, ensuring that clinical research protocols are adhered to.
• Maintain supplies, including lab kits and reorder them as necessary.

We offer a great benefits package that includes vacation/sick pay, holiday pay, scrub allowance annually, 401k/profit sharing, on demand pay, medical, dental, vision benefits etc.

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