Senior Clinical Research Coordinator
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. The incumbent is responsible for 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. Attends clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, etc. Incumbent will ensure study protocols are followed, appropriate documentation is kept, and accurate data is collected. Incumbent will be responsible for the preparation and submission of study documents to the Institutional Review Board (IRB), Sponsored Projects Administration (SPA) and other regulatory committees.
Requirements
- Demonstrated high-level communication skills to convey information in a clear and concise way,synthesizing information and presenting it to others.
- 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.
- 3-5 years
Nice To Haves
- Advanced degree (MA, MS, or MPH) preferred
- Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.
Responsibilities
- 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
- 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
- Attends clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, etc
- ensure study protocols are followed, appropriate documentation is kept, and accurate data is collected
- responsible for the preparation and submission of study documents to the Institutional Review Board (IRB), Sponsored Projects Administration (SPA) and other regulatory committees.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
11-50 employees
