COMPANY DESCRIPTION
Unio Health Partners (UHP) is a highly differentiated physician practice management platform with the goal of transforming care delivery across the Western United States. UHP partners with leading physician practices, creating a cohesive, quality-oriented clinical culture and facilitating best practice sharing across the platform. Our affiliated practices gain access to a broader suite of services, providing a meaningful benefit to both physicians and patients. UHP's best-in-class clinical program covers three sub-specialties (urology, gastroenterology, and radiation oncology) and offers numerous ancillary services, including pathology lab, in-office dispensing, and chronic care management. We are led by a highly accomplished management team and provide a full suite of management services to its affiliated practices. UHP is currently affiliated with 182 providers consisting of 119 physicians and 63 advanced practice providers operating out of 54 locations across Southern, Central, and Northern California.
POSITION SUMMARY
The Clinical Research Coordinator is a specialized research professional working with and under the direction of the clinical Principal Investigator and supports, facilitates and coordinates the daily clinical trial activities. The Clinical Research Coordinator works with the Principal Investigator, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study. Communication with staff in all departments is paramount in this position, ensuring that the clinical research study needs of all departments are met effectively and efficiently.
What you will be doing
- Coordinate with Principal Investigator and department to help ensure that clinical research and related activities are performed in accordance with federal regulations and Institution and sponsoring agency policies and procedures.
- Assist the Principal Investigator in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
- Assist Principal Investigator in protection of the rights and welfare of all human research participants involved in research in accordance with federal regulations and Institution and sponsoring agency policies and procedures.
- Attend investigator meetings as required or requested by the Principal Investigator.
- Collaborate with Principal Investigator and institution to respond to any audit findings and implement approved recommendations.
- Review and accept/correct the billing matrix as set up by the Research Director to facilitate billing of study procedures to the appropriate research fund.
- Collect documents needed to initiate the study and submit to the sponsor.
- Coordinate participant tests and procedures.
- Complete study documentation and maintain study files in accordance with sponsor requirements and Institution policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
What you will bring to the team
- Bachelor's degree in a scientific discipline preferred or CRC certified for the past 4 years or over 8 years of clinical research experience in a Clinic Setting.
- Basic Life Support, Certified Phlebotomist Tech I, or a Medical Assistant Certification.
- Active CCRC, CCRP, GCP or ICH certification preferred.
- 5+ years of Cancer/Urology clinical research experiencein a private practice setting required.
- Skilled in phlebotomy
- Experience working with clinical trial management software.
- Experienced with inpatient and outpatient protocols.
- Appropriate knowledge of anatomy, physiology, disease process and standard treatment protocols.
- Working knowledge of clinical research policies and procedures, IRB's, and FDA regulatory requirements for clinical studies
What we can offer you
- Competitive Salary and Health Benefits (Medical, Dental, Vision)
- Generous time off (start accruing on your first day - no waiting period)
- Paid Holidays
- 401(k)
- Company Discounts
- Collaborative work environment - we want our employees to have a say in how we run our office
- Employee Recognition
Compensation is depending on a number of factors including a candidate's qualifications, skills, competencies, or experience that may fall outside of the range shown
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