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Specimen Processing Specialist II

Remote: 
Full Remote
Contract: 
Salary: 
58 - 58K yearly
Experience: 
Mid-level (2-5 years)
Work from: 
Texas (USA), United States

Offer summary

Qualifications:

High School degree or equivalent required., 3+ years of laboratory data entry experience., Knowledge of medical terminology and medications., Typing speed of at least 45 wpm., Ability to multi-task in a fast-paced environment..

Key responsabilities:

  • Verify patient demographics and specimens.
  • Identify problems and engage Client Services.
  • Accurately enter patient information into LIS.
  • Learn job duties and understand departmental functions.
Fulgent Genetics logo
Fulgent Genetics Biotech: Biology + Technology SME https://www.fulgentgenetics.com/
201 - 500 Employees
See more Fulgent Genetics offers

Job description

Job Details
Level:    Entry
Job Location:    Undisclosed
Education Level:    High School
Salary Range:    Undisclosed
Job Category:    Biotech
Description

About Us

Inform Diagnostics, a Fulgent Genetics Company, is a nationally recognized diagnostics laboratory focused on anatomic pathology subspecialties including gastrointestinal pathology, dermatopathology, urologic pathology, hematopathology, and breast pathology.

Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier, full-service genomic testing company built around a foundational technology platform.

Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.

Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.

 

Summary of Position

The Specimen Processing Specialist II is responsible for general support functions within the Specimen Processing Department. All functions must be performed with confidence, accuracy and in a timely manner. This position is critical to quality for customer satisfaction. Department is a production environment, with emphasis on productivity/quality standards and departmental completion times.

 

Key Job Elements

  • Verify patient demographics, physician data, tests requested, time and date of collection, appropriate clinical information and all other pertinent data found on laboratory request forms.
  • Identifies problems with specimen types, missing information etc. and engages Client Services department to resolve them.
  • Accurately enters patient information into laboratory information system (LIS).
  • Demonstrates an ability to learn the job duties assigned, and develops an understanding of how all the functions in Specimen Processing fit together.
Qualifications

Knowledge/Experience

  • High School degree or equivalent required.
  • 3 plus years previous laboratory and medical data entry experience.
  • Skills, such as experience in data entry, high attention to detail, and focus on quality are a must.
  • Knowledge of medical terminology and medications.
  • Typing speed of at least 45 words per minute with a high accuracy rate.
  • Ability to multi-task and work in a fast-paced, deadline driven environment.
  • Ability to decipher various forms of handwriting.
  • Excellent skills in English usage, grammar, punctuation, and spelling.
  • Maintains composure while working under pressure.
  • Reflects good judgment at all times when determining what action to take when resolving problems.
  • Manual dexterity to use common laboratory equipment and perform sterile techniques as required.

 

Lab Specific Qualifications

  • Visual acuity (including color discrimination) and analytical skill to distinguish fine detail.
  • Ability to tolerate extensive periods seated and/or standing.
  • Must possess ability to perform repetitive motion.
  • Ability to lift up to 30 pounds.
  • May have exposure to extreme temperatures, high noise levels, fumes and bio-hazardous material/chemicals including formalin in the lab environment.
  • May be required to handle blood-borne pathogens and general laboratory reagents; handle live human specimens, tissues, and bodily fluid.

 

Environment

Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term “qualified individual with a disability” means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.

This job description reflects management’s assignment of essential functions. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

For California residents, please see the link below to access our CCPA Privacy Notice.

CCPA Privacy Notice for California Residents

https://tinyurl.com/FulgentCCPA

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
EnglishEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Multitasking
  • Problem Solving
  • Detail Oriented
  • Typing
  • Verbal Communication Skills
  • Finger Dexterity
  • Analytical Skills
  • Time Management

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