Non-Clinical - Administrative - Clinical Research Assistant
Non-Clinical - Administrative - Clinical Research Assistant
Posted on :
18-08-2025
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1 Vacancy
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Job Description
Job Summary:
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.
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.
- 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.
- 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).
- 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.
- 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.
Employment Type
Full-time
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