Senior Clinical Research Coordinator

UCI Health • Orange, CA

235d

About The Position

Under the direction of the Assistant Director of Clinical Research Operations, the Senior Clinical Research Coordinator will be responsible for supporting clinical research efforts of the UCI Alpha Clinic (AC) by providing comprehensive coordination and data management of sponsored clinical trials according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures.

Requirements

• Demonstrated high-level communication skills to convey information in a clear and concise way
• Demonstrated problem solving capabilities to resolve concerns that arise unexpectedly
• Demonstrated ability to research, properly evaluate information, and prepare concise, well organized reports, summaries, and correspondence
• Demonstrated ability to organize and prioritize a complex and dynamic workload
• Ability to multitask and meet deadlines, despite interruptions
• Ability to independently exercise discretion and sound judgment
• Ability to work collegially and cooperatively in a small office and to establish and maintain cooperative working relationships
• Demonstrated skill in interacting with persons of various social, cultural, economic and educational backgrounds
• Ability to prioritize assignments and achieve high productivity/quality with short time frames, under rigid deadlines, and /or in environments with frequent workload changes and competing demands
• Skill in working independently, taking initiative and following through on assignments
• Ability to think critically, compile data from various sources, analyze data, and prepare reports
• High level of integrity and honesty in maintaining confidentiality
• Foster and promote a positive attitude and professional appearance
• Strong attention to detail
• Working knowledge of computer software including Microsoft Office (Outlook, Word, Excel, and PowerPoint)
• Experience with a nationally-recognized clinical research coordinator certification
• Bachelor's degree in related area and / or equivalent experience / training

Nice To Haves

• Advanced degree (MA, MS, or MPH)
• Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals

Responsibilities

• Supporting and coordinating all aspects of UCI AC trials and studies for protocol specific requirements, research procedures, research chart preparation, data collection, subject study management and record keeping
• Attending clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, etc.
• Ensuring study protocols are followed, appropriate documentation is kept, and accurate data is collected
• Preparing and submitting study documents to the Institutional Review Board (IRB), Sponsored Projects Administration (SPA) and other regulatory committees

Benefits

• Medical insurance
• Sick and vacation time
• Retirement savings plans
• Access to a number of discounts and perks

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Hospitals
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees