Job Title: Clinical Trials Specimen Management Technician
Department: Specimen Processing
Location: Onsite, York, UK
Hours Per Week: 37.5
Schedule: Monday - Friday, 9:00 AM - 5:00 PM OR Tuesday - Saturday, 8:00 AM - 4:00 PM
SUMMARY
The Clinical Trials Specimen Management Technician I performs the daily operations of specified areas within the Clinical Trials Specimen Management (CTSM) Laboratory. They perform all daily functions in accordance with company policies and procedures.
RESPONSIBILITIES
- Perform all processes in accordance with SOP’s and appropriate regulatory guidelines
- Perform receipt, QC checks and onward processing for Clinical Trials specimens
- Perform accurate data entry into various laboratory information management systems
- Prepare samples for onward shipment
- Work with samples under varying temperature conditions including ultra-cold (-80°C) and liquid nitrogen (-196°C)
- Handle deliveries of packages including lifting and carrying of boxes filled with dry ice
- Perform housekeeping as required to maintain a clean and tidy working environment including frozen storage unit maintenance and emptying waste ice receptacles
- Utilize study documentation to aid in problem solving and elevate to senior staff as required
- Manage specimen related study documentation including preparation for archiving
- Guarantee client satisfaction by providing exceptional service to internal customers
- Adapt to changing priorities with guidance from senior team members
- Perform specimen receipt/accessioning/shipping activities depending on your main area of work (Routine, storage or batched shipping) including but not limited to
- Utilize Environmental monitoring software to monitor all specimen storage units to always ensure integrity of all specimens
- Perform other duties as assigned
REQUIRED QUALIFICATIONS
GCSE
PREFERRED QUALIFICATIONS
- Strong Microsoft Office and data entry skills
- Strong attention to detail
- Works well in group setting as well as individually
- Strong communication skills
PHYSICAL REQUIREMENTS:
Moderate - These roles require a combination of movement and stationary work, including frequent standing, walking, and moderate lifting (up to 50 lbs.). Tasks may involve repetitive reaching, bending, pushing, or pulling, along with maintaining awareness in high-traffic or operational areas. Visual focus and spatial awareness are critical in facilities, logistics, or support settings. Emotional demands include managing interruptions, prioritizing tasks, and maintaining compliance with safety standards. Environmental exposures may include equipment noise, shared workspaces, and occasional proximity to hazardous areas. Physical capability screening may be required.
Rochester Regional Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, national origin, age, disability, predisposing genetic characteristics, marital or familial status, military or veteran status, citizenship or immigration status, or any other characteristic protected by federal, state, or local law.
At ACM Global Laboratories, we understand that every project we work on, every task we complete impacts patients and their families. Our dedication to being purposefully patient-driven is reflected in the high-quality work provided by our teams every day around the globe.
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Clinical Trials Specimen Management Technician employer: 955 ACM UK
ACM Global Laboratories is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of the United Kingdom. With a strong commitment to employee growth, we provide ample opportunities for professional development and training, ensuring that our team members are equipped to excel in their roles. Our focus on quality and adherence to regulatory standards creates a meaningful environment where you can make a significant impact in the field of analytical R&D.