What are the responsibilities and job description for the Clinical Research Medical Assistant position at Urology Associates Of Central California Medical Group Inc?
Urology Associates Of Central California is currently looking for a Clinical Research Medical Assistant to join our team. We are looking for someone with a medical assisting background who can handle patient care procedures, such as blood draws and EKGs, while also supporting research activities. Two year of experience needed.
The Clinical Research Medical Assistant performs a variety of clinical study activities to assist the Clinical Research Coordinators 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.
- Coordinate protocol related research procedures, study visits, and follow up care
- Phlebotomy experience preferred
- Experience in clinical research or a willingness to learn clinical research practices.
- strong critical thinking and problem solving skills.
- Ability to work independently and as part of a team with attention to detail.
- 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.
- 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.
- 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.
Salary : $18 - $23
