Asst. Biospecimen Coordinator

University of California, IrvineOrange, CA
4d

About The Position

Under the supervision of the Biospecimen Lab Manager, the Assistant Biospecimen Coordinator (ABC) supports the clinical research efforts by coordinating and processing biological specimens for cancer related protocols according to current Good Clinical Practices (GCP), Good Laboratory Practices (GLP), internal standard operating procedures (SOPs) and University policies and procedures. The incumbent is responsible for supporting all aspects of the study specimen process for patients participating in cancer related clinical trials, which includes: collecting, processing, storing, shipping, and tracking under specific research protocol requirements and laboratory techniques. In addition, this individual is responsible for providing general maintenance and organization of the Cancer Center research laboratory. This includes: maintaining laboratory equipment, ordering supplies, tracking equipment service agreements, ensuring proper equipment operation, and maintaining and updating standard operating procedures.

Requirements

  • Experience working with and processing biological specimens
  • Experience working in a clinical laboratory environment
  • Experience with clinical research and data collection
  • Ability to interact with the public, faculty, and staff
  • Ability to establish and maintain files and records
  • Strong organizational and verbal communication skills
  • 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
  • Ability to think critically, compiles data from various sources, analyze data, and prepare reports.
  • Ability to work both independently and as part of team
  • Ability to take initiative and demonstrate strong commitment to duties
  • Ability to analyze problems, implement solutions and multitask
  • Ability to work within a deadline-driven structure
  • Demonstrated experience in maintaining flexibility and adaptability while implementing institutional change
  • 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
  • 1-3 Years of related work experience with Bachelor of Arts/Bachelor of Science, or
  • Experience working with and processing biological specimensequivalent experience
  • Experience working in a clinical laboratory environment
  • Experience with clinical research and data collection

Nice To Haves

  • Experience with cancer-related research.
  • Extensive experience with various types of human subject clinical trials i.e., National Group, Industrial, and Investigator-authored.
  • Experience with clinical trial management systems, preferably OnCore.

Responsibilities

  • collecting, processing, storing, shipping, and tracking under specific research protocol requirements and laboratory techniques
  • maintaining laboratory equipment
  • ordering supplies
  • tracking equipment service agreements
  • ensuring proper equipment operation
  • maintaining and updating standard operating procedures

Benefits

  • medical insurance
  • sick and vacation time
  • retirement savings plans
  • access to a number of discounts and perks

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Number of Employees

101-250 employees

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