Clinical Research Medical Assistant at Urology Associates Of Central California Medical Group Inc Fresno, CA

Benefits

Qualifications

• •s familiar with the medical field
• •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
• •At least 2 years of clinical research coordinating experience
• •Knowledge of GCP, federal state and local regulations, including HIPPA policies and procedures
• •3 more items(s)

Responsibilities

• •The Clinical Research Coordinator performs a variety of clinical study activities to assist the Principal Investigator in the conduct of a clinical study
• •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
• •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
• •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
• •20 more items(s)