Specimen Management Technician
Altasciences
Summary
The Specimen Management Technician, working under direct supervision, is responsible for the timely and accurate receipt, preparation, management, processing, shipping and/or storage of laboratory specimens in compliance with GLP guidelines, study protocols and SOPs.
Job description
About the Role
The Specimen Management Technician, working under direct supervision, is responsible for the timely and accurate receipt, preparation, management, processing, shipping and/or storage of laboratory specimens in compliance with GLP guidelines, study protocols and SOPs.
What You’ll Do Here
- Responsible for working in compliance with GLP guidelines, protocols and SOPs.
- Coordinate with study directors, coordinators, pathologists, laboratory staff, and vivarium staff.
- Prepare, receive, centrifuge, separate and transfer/ship specimens according to SOPs and protocol design with limited supervision.
- Maintain and utilize laboratory equipment and instruments.
- Maintain chain of custody of all specimens processed and ensure timely transfer of specimens for analysis, archive, shipment or storage.
- Maintain documentation of procedures and equipment used and performs quality control of forms and logs.
- Maintain laboratory/shipping supplies.
- Maintain cleanliness of the department areas.
- Cross-train to perform other duties within specimen management.
- Assist all areas of specimen management as well as other departments.
What You’ll Need to Succeed
- High school diploma or equivalent required.
- Previous laboratory or regulated environment preferred.
- Knowledge of current International Air Transport Association (IATA) and Code of Federal Regulations (49 CFR) transportation safety requirements preferred.
- Basic computer skills including proficiency with Microsoft Office suite; adapts easily to new software.
- English proficiency both written and verbal; general reading, writing and verbal communication skills.
- High level detail-orientation with problem solving and troubleshooting skills required.
- Strong communication skills preferred.
- Basic math skills.
- Watson system knowledge preferred.
- Strong cross-team collaboration.
- Flexibility and efficiency in a fast-paced environment.
Requirements
- High school diploma or equivalent required.
- Previous laboratory or regulated environment preferred.
- Knowledge of current International Air Transport Association (IATA) and Code of Federal Regulations (49 CFR) transportation safety requirements preferred.
- Basic computer skills including proficiency with Microsoft Office suite; adapts easily to new software.
- English proficiency both written and verbal; general reading, writing and verbal communication skills.
- High level detail-orientation with problem solving and troubleshooting skills required.
- Strong communication skills preferred.
- Basic math skills.
- Watson system knowledge preferred.
- Strong cross-team collaboration.
- Flexibility and efficiency in a fast-paced environment.
Benefits
- Health/Dental/Vision Insurance
- 401(k) with Employer Match
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Employee Assistance & Telehealth Programs
- Telework when applicable
- Training & Development Programs
- Employee Referral Bonus Program
Company overview
Altasciences is a forward-thinking, mid-size contract research organization (CRO) and contract development manufacturing organization (CDMO) that provides integrated, full-service solutions for early phase drug development. Founded in 1992 and owned by Novo Holdings A/S, the company offers pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies. Their comprehensive services include preclinical safety testing, clinical pharmacology and proof of concept studies, bioanalysis, formulation development, manufacturing and analytical services, program management, medical writing, biostatistics, and data management. With over 1,800 employees across eight facilities in the U.S. and Canada, Altasciences has established itself as a trusted partner for drug development from lead candidate selection through clinical proof of concept and beyond. The company's integrated CRO/CDMO model enables seamless transitions between development phases, reducing complexities, mitigating risks, and accelerating timelines for clients ranging from startups to global pharmaceutical leaders.