Regulatory Affairs Coordinator - Irvine, United States - University Of California Irvine

Description

Job Opening ID: 66133 Reports To: Director - Clinical Research Operations Working Title: Regulatory Affairs Coordinator Department: UCI Ctr for Clinical Research Bargaining Unit: RX FLSA: Non-Exempt Payroll Job Code: Job Location: UCI Campus- Irvine Percent of Time: 100% Work Schedule: 8-5, M-F Employee Class: Career Position Summary: The UCI Center for Clinical Research was built on the belief that running clinical trials should be a seamless experience. We work across the UCI enterprise to offer patients, investigators, and industry partners the quick and effortless support they need to participate in and run successful clinical trials. Our goals are to: Innovate - capitalized on opportunities by developing fresh ideas and innovative approaches to improving our daily work. Accelerate - Work as a team of teams, driving process simplification, and standardization to surpass our study activation and enrollment targets. Grow & Inspire - Set the industry bar for world-class experiences for each other, our patients and partners, and elevate our brand as high performers. For more information on CCR, please visit our website at
The Regulatory Affairs Coordinator position will ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research.
Total Compensation:

In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our compensation practices and benefits.

The expected pay range for this recruitment is $ $52.92 (Hourly Rate). The Full Salary Range for the salary grade this position is assigned to is $ $52.92 (Hourly Rate). Required:

• 1-3 years as a Regulatory Affairs Coordinator or the equivalent education or experience
• Associates or Bachelor's Degree. Or the equivalent experience.
• 2-3 years of experience with regulatory aspects of clinical research including maintaining regulatory documents, submitting IRB application, and working with study sponsors and monitors.
• Basic knowledge of Microsoft Word, Excel, PowerPoint Demonstrated problem solving capabilities
• Excellent interpersonal communication skills, both oral and written
• Ability to work under minimal supervision and know how to escalate to proper authorities when needed.
• Ability to comprehend complex documents such as study protocols, guidance documents, and study manuals then synthesize information.
• Ability to prioritize tasks when different stakeholders involved and with competing priorities and deadlines.
• Ability to work well with teams both within and outside of department
• Ability to travel to both medical center in Orange or to main office site in Irvine

Preferred:

• CCRP preferred, but not required
• Experience with IND submission Experience as a clinical research coordinator and/or familiar with the clinical side (versus the regulatory side) of a study.
• Experience with CTMS, preferably OnCore CCRP Certified through one of the national clinical research associations (SOCRA or ACRP) or willing to become certified Familiar with FDA Inspection process

Special Conditions Preferred:
* Ability to travel to either Orange Medical Center or main office in Irvine

Conditions of Employment:

The University of California, Irvine (UCI) seeks to provide a safe and healthy environment for the entire UCI community. As part of this commitment, all applicants who accept an offer of employment must comply with the following conditions of employment:

• Background Check and Live Scan
• Legal Right to work in the United States
• Vaccination Policies
• Smoking and Tobacco Policy
• Drug Free Environment

The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements.

• California Child Abuse and Neglect Reporting Act
• E-Verify
• Pre-Placement Health Evaluation

Details of each policy may be reviewed by visiting the following page -

Closing Statement:

The University of California, Irvine is an Equal Opportunity/Affirmative Action Employer advancing inclusive excellence. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC nondiscrimination policy.
We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.
UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at or