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Clinical Research Assistant Full Time
4 months ago
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.
We offer a great benefits package that includes vacation/sick pay, holiday pay, scrub allowance annually, 40k/profit sharing, on demand pay, medical, dental, vision benefits etc.