The Assistant Biospecimen Coordinator (ABC) supports clinical research by coordinating and processing biological specimens for cancer-related protocols, adhering to GCP, GLP, SOPs, and university policies. Responsibilities encompass the entire specimen lifecycle (collection, processing, storage, shipping, tracking) and general laboratory maintenance (equipment upkeep, supply ordering, SOP updates). The role requires strong organizational, communication, and problem-solving skills, along with the ability to work independently and collaboratively within a team.
Location: Orange, California, United States,
Responsibilities:
- Coordinate and process biological specimens for cancer research protocols.
- Collect, process, store, ship, and track specimens according to research protocol requirements.
- Maintain and organize the Cancer Center research laboratory.
- Maintain laboratory equipment, order supplies, and track service agreements.
- Ensure proper equipment operation and update standard operating procedures.
- Interact with patients, faculty, and staff.
- Maintain files and records.
- Prepare reports and summaries.
- Organize and prioritize workload, meeting deadlines despite interruptions.
- Exercise discretion and sound judgment.
- Collaborate effectively with team members.
- Analyze problems and implement solutions.
- Maintain confidentiality.
- Foster a positive attitude and professional appearance.
Required Skills & Certifications:
- Experience working with and processing biological specimens.
- Experience working in a clinical laboratory environment.
- Experience with clinical research and data collection.
- Strong organizational and verbal communication skills.
- Ability to interact effectively with diverse individuals.
- Demonstrated problem-solving and critical thinking skills.
- Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint).
- 1-3 years of related work experience with a Bachelor of Arts/Bachelor of Science degree, or equivalent experience.
Preferred Skills & Certifications:
- Experience with cancer-related research.
- Experience with various types of human subject clinical trials (National Group, Industrial, Investigator-authored).
- Experience with clinical trial management systems (preferably OnCore).
Special Considerations:
- The role operates within a clinical research laboratory environment. Adherence to GCP and GLP is mandatory.
Scheduling:
- The job description does not specify scheduling details.
...for BaRupOn's infrastructure development projects. This associate- or early-career-level position involves analyzing market trends, tracking regulatory developments, and supporting economic assessments of power generation, energy storage, and grid infrastructure...
...Job Title: Business Analyst (Data Governance and Data Quality Management) Location: Auburn Hills, MI. Must be local or relocation (out of pocket from day 1). No exceptions. HEAVY preference for locals in this group. NO West Coast candidates (PST) will be considered...
...Archdiocese of Saint Louis. Job Summary Job Title: IT Help Desk Technician Ministry: Cardinal Ritter Senior Services Reports... ...troubleshooting IT systems, hardware, and software Strong working knowledge of Microsoft tools: Teams, Defender, Purview, O365,...
...opportunities within the organization Job Description The Behavioral Tech is responsible for observing and reporting on client... ...and clean. Knowledge of drug and alcohol dependency, mental health, family systems and various recovery resources in the community...
Class A CLASS A ETHANOL TANKER DRIVER - GREAT SCHEDULE - GREAT PAY - GREAT BENEFITS JobExperienced Class A driver, must have Tanker and... ...before we will train you to haul ethanol! We can be flexible and come up with a schedule that works for you - Like 4 on and 4 off - or...