- 5 to 7 Years of related clinical research coordination work experience with Bachelor of Arts/Bachelor of Science, or equivalent experience
- 5 to 7 Years of related clinical research coordination work experience with Bachelor of Arts/Bachelor of Science, or equivalent experience
- Ability to interact with the public, faculty, and staff
- Ability to establish and maintain files and records
- Access to transportation to off-site research locations
- Willingness to work as a supportive, cooperative member of an interdisciplinary team
- 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
- May require study management coordination outside of normal business hours. May require travel to satellite sites.
- Background Check and Live Scan
- Legal Right to work in the United States
- Vaccination Policies
- Smoking and Tobacco Policy
- Drug Free Environment
- California Child Abuse and Neglect Reporting Act
- E-Verify
- Pre-Placement Health Evaluation
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Clinical Research Coordinator
2 weeks ago
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Clinical Research Coordinator
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Clinical Research Coordinator
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University Of California Irvine Orange, United States· Job Opening ID: 59646 Reports To: Clinical Research Manager of the Clinical Trials Unit Working Title: Clinical Research Coordinator - Hybrid Department: Cancer Center Bargaining Unit: RX FLSA: Non-Exempt Payroll Job Code: Job Location: UCI Campus- Irvine Percent of Time: 100% ...
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Clinical Research Coordinator
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Asst. Research Data Coordinator
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UCI Health Orange, United StatesJob Opening ID: 62908 · Reports To: Clinical Research Manager · Working Title: ASST. RESEARCH DATA COORDINATOR - HYBRID · Department: Cancer Center · Bargaining Unit: RX · FLSA: Non-Exempt · Payroll Job Code: 009336 · Job Location: UCI Campus- Irvine · Percent of Time: 100% · Wor ...
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Assistant. Clinical Research Coordinator
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Assistant Clinical Research Coordinator
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UCI Health Orange, United StatesJob Opening ID: 59648 · Reports To: Clinical Research Manager of the Clinical Trials Unit · Working Title: Assistant Clinical Research Coordinator - Hybrid · Department: Cancer Center · Bargaining Unit: RX · FLSA: Non-Exempt · Payroll Job Code: 009336 · Job Location: UCI Campus- ...
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Asst. Research Data Coordinator
2 weeks ago
UCI Health Orange, United StatesJob Opening ID:62928 · Reports To: Clinical Research Manager · Working Title: Asst. Research Data Coordinator - Hybrid · Department: Cancer Center · Bargaining Unit: RX · FLSA: Non-Exempt · Payroll Job Code: 009336 · Job Location: UCI Campus- Irvine · Percent of Time: 100% · Work ...
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Assistant. Clinical Research Coordinator
2 weeks ago
UCI Health Orange, United StatesJob Opening ID: 60800 · Reports To: Clinical Research Manager · Working Title: Assistant. Clinical Research Coordinator - Hybrid · Department: Cancer Center · Bargaining Unit: RX · FLSA: Non-Exempt · Payroll Job Code: 009336 · Job Location: UCI Campus- Irvine · Percent of Time: 1 ...
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Clinical Research Coordinator Assistant
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University Of California Irvine Orange, United States· Job Opening ID: 64901 Reports To: Assistant Professor in Residence Working Title: Clinical Research Coordinator Assistant Department: Peds Developmental & Behav Bargaining Unit: RX FLSA: Non-Exempt Payroll Job Code: Job Location: Orange, UCI Medical Center Percent of Time: 100 ...
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Clinical Research Coordinator Assistant
2 weeks ago
UCI Health Orange, United StatesJob Opening ID: 69045 · Reports To: Assistant Professor In Residence · Working Title: Clinical Research Coordinator Assistant · Department: Peds Developmental & Behav · Bargaining Unit: RX · FLSA: Non-Exempt · Payroll Job Code: 009336 · Job Location: UCI Campus- Irvine · Percent ...
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Clinical Research Coordinator
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Clinical Research Coordinator
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Orange County Neuropsychiatric Rese Orange, United StatesJob Description · Job DescriptionNRC Research Institute has been conducting clinical trials for the worlds pharmaceutical firms since 2004. We specialize in pharmaceutical clinical trials involving CNS (Central Nervous System) disorders such as Schizophrenia, Bipolar Disorder, De ...
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Clinical Research Coordinator
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Orange County Neuropsychiatric Rese Orange, United StatesJob Description · Job DescriptionNRC Research Institute has been conducting clinical trials for pharmaceutical and biotech companies since 2004. We specialize in pharmaceutical clinical trials involving Central Nervous System disorders such as Schizophrenia, Bipolar Disorder, Dep ...
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Clinical Research Coordinator
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Clinical Research Coordinator
3 weeks ago
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Clinical Research Coordinator
3 weeks ago
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Children's Hospital of Orange County Orange, United StatesWork Location · Orange, California · Work Shift · Day - 08hrs (United States of America) · Why CHOC? · At CHOC, we strive to be the leading destination of children's health by providing exceptional and innovative care. We are responsible for the overall health of our community's ...
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Clinical Research Coordinator
1 week ago
Clemente Clinical Research Santa Ana, United StatesJob Description · Job Description · Job Description: · As the experienced Clinical Research Coordinator Manager at Clemente Clinical Research, you will work with a team that is dedicated to bringing quality care to those in the community who need it most. The majority of our pa ...
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Children's Hospital of Orange County Orange, United StatesWork Location · Orange, California · Work Shift · Day - 08hrs (United States of America) · Why CHOC? · At CHOC, we strive to be the leading destination of children's health by providing exceptional and innovative care. We are responsible for the overall health of our community's ...
sr. clinical research coordinator - Orange, United States - University Of California Irvine
Description
Job Opening ID: 67959 Reports To: Clinical Research Manager Working Title: SR. CLINICAL RESEARCH COORDINATOR - HYBRID Department: Cancer Center Bargaining Unit: RX FLSA: 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 NCI-designated Chao Family Comprehensive Cancer Center (CFCCC) is a campus-wide multidisciplinary matrix organization whose goal is to promote and enhance cancer-relevant research and patient care at UC Irvine. The CFCCC provides research resources to its ~175 members engaged in research and offers multidisciplinary cancer care to its patients.
Under the supervision of the Clinical Research Manager (CRM) within the Clinical Trials Unit, the Senior Clinical Research Coordinator (SCRC) supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management for complicated Phase I-IV cancer protocols 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 the cancer-related trials (Phase I-IV) for protocol specific requirements, research procedures, research chart preparation, data collection, and record keeping. Attends clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, answer research patient questions, schedule appointments, etc. Serve as the liaison to sponsors, governing agencies and facilitate transmission of verbal and written communication to national cooperative oncology groups, pharmaceutical companies and other research entities as needed. The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. The incumbent is responsible, under the direction of the CRM, to provide training and guidance to other clinical research coordinators, demonstrating best practices, and provides ongoing analysis of internal processes and provides recommendations for new policies and procedures to improve overall operational efficiency and customer service. The incumbent is responsible, under the direction of the CRM, for leading and managing pre-study site selection visits (PSSVs) including liaising with all appropriate ancillary medical service units (e.g., Investigational Drug Service, Pathology, Radiology, etc.) for the conduct of the trial for the assigned disease area. In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI). 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.
$ $64.04 (Hourly Rate) Department Website:UCI Chao Family Comprehensive Cancer Center
Required: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:
The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements.
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
