Laboratory Assistant

The Laboratory Assistant is primarily responsible for performing duties within the laboratory related to receiving sample shipments accessioning and performing data entry into laboratory systems management of samples manual processing and handling of samples clerical duties to support laboratory operations and other miscellaneous tasks.

Laboratory Assistant responsibilities include but are not limited to the following:

• Receive accessions labels or rejects specimens by following standard operating procedures (SOPs).
• Interpret sample requisition forms and other related documentation and if information is discrepant or missing; obtain required information.
• Perform data entry of case information into the appropriate computer system ensuring that all identifying information is accurate and in the appropriate format.
• Perform manual processing of samples in the laboratory including but not limited to sample aliquoting ThinPrep processing cell block preparation staining and coverslipping.
• Prepare specimens for analysis
• Perform all housekeeping duties and laboratory cleaning as required.
• Under direction of the laboratory management ensure that lab supplies are ordered and stocked to avoid any lapses in specimen processing and/or testing.
• Maintain inventory documentation and communicate to laboratory management when there are delays in supply delivery to the lab.
• Performs quality control checks and troubleshoots instrumentation.
• Utilizes maintains troubleshoots and documents equipment maintenance according to checklist to ensure proper performance of equipment.
• Adhere to SOPs policies work instructions and protocols in the lab.
• Obtains samples and files in numerical order where applicable in correct location based on type and project.
• Follows laboratory regulation guidelines to file retain or destroy tissue blocks slides vials logs and paperwork.
• Participate in safety and compliance training on a regular basis.
• Participate actively in all laboratory quality management and quality assurance functions.
• Ability to read interpret and comply with documents such as internal SOPs operating and maintenance instructions and company policies.
• Disposes of and properly handles sharps reagents biological and/or hazardous waste in a manner that is consistent with laboratory state and federal government regulations.
• Participates when requested in training/teaching new employees.
• Respects the confidentiality of client and patient records.
• Coordinates workload with other lab assistants and technologists to maximize productivity and quality of work based upon metrics.
• Complete all procedures expected in the scheduled time without loss of work quality.
• Notify management regarding trends changes or problems as they occur.
• Performs activities in accordance with regulatory requirements as defined by appropriate QCD (ID#: 887) for high complexity testing personnel (This item is preferred but not required)

Qualifications :

Basic Minimum Educational Requirements:

• High school diploma or GED acceptable Associate or Bachelor of Applied Science preferred.

Basic Minimum Qualifications:

• Minimum 0-2 years experience 
• Meet CLIA 88 qualifications to perform moderate complexity testing as described in Sec. 493.1423 is required.
  • Meet additional qualifications to perform high complexity testing as described in Sec. 493.1489 is preferred.
• Authorization to work in the United States indefinitely without restriction or sponsorship. 

The Ideal Candidate Possesses the Following:

• Ability to work in a fast-paced laboratory environment
• Strong organization skills
• Ability to handle multiple tasks simultaneously.
• Strong analytical logistics leadership and communication skills; verbal and written.
• Ability to think logically to troubleshoot analyze situations and make appropriate decisions.
• Proficient computer skills including working knowledge of Microsoft Office Suite e-mail systems (Outlook) and web-based programs.
• Knowledge of current medical terminology to perform various laboratory tests and to communicate with laboratory staff other departments and clinical trial site staff.
• Ability to occasionally push pull lift move and/or carry up to 40lbs. 
• Knowledge of safety requirements to provide instructions and to recognize hazardous conditions.
• Punctual and is consistently at work and on time.
• Wear personal protection equipment/attire provided and be able to complete job functions.
• Good speaking and listening skills.
• Ability to perform focused work with close attention to detail.
• The noise level in the work environment is low-moderate.

Additional Information :

Position is full-time working Monday - Friday 9:00am - 5:00pm with overtime as needed.  Candidates currently living within a commutable distance of Carmel IN are encouraged to apply.

• Excellent full-time benefits including comprehensive medical coverage dental and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

No

Employment Type :

Full-time