Clinical Sample Processor I

Job content

• Recognize, exemplify and adhere to ICON’s values which centre’s around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Responsible for data entry of patient’s demographics into the computer system. Documents and researches any problems with received specimens including off line order entry. Adheres to OSHA and the Company’s Health and Safety regulations and security procedures at all times. Understands the principles and accreditation and QA procedures. Understands the principles of accreditation and QA procedures
• Store in samples based on protocol specifications, as well as accountability for storage samples
• Quality checking of accession forms, scanning of paperwork into database. Archiving visit documentation
• Bar code labelling and validation of specimens and transport of specimens to the technicians in the laboratory to be analyzed
• Facilitate removal and collection of all hazardous waste from laboratory
• Escalating any problems to senior members of the team
• Additional responsibilities as request by management of Sample Management

• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• One to two years of relevant experience*
• Basic working knowledge of computers and accuracy and attentiveness to detail necessary.
• An alternate combination of experience, education, and training determined by management to be equivalent to the foregoing.

• High School Diploma/Leaving Certificate/diploma in Life Sciences or administrative computer related field.