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Clinical Pathology Services Manager

Tpainc

Arkansas

On-site

USD 70,000 - 90,000

Full time

Today
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Job summary

A leading clinical pathology firm in Jefferson, Arkansas, is looking for a Clinical Pathology Services Manager to oversee laboratory operations and staff. This role requires a Bachelor’s degree in Medical Laboratory Sciences and at least two years of clinical laboratory experience. The position involves collaboration with research investigators and compliance with FDA regulations in a dynamic work environment. An attractive benefits package and competitive salary are offered.

Benefits

Comprehensive benefits package
Competitive salary

Qualifications

  • Bachelor's degree from an accredited institution.
  • Minimum two years experience in a clinical pathology laboratory.
  • Successful completion of military training as Medical Laboratory Specialist is a plus.

Responsibilities

  • Oversee laboratory operations and staff.
  • Collaborate with NCTR investigators for testing.
  • Ensure compliance with FDA/EPA regulations.

Skills

Leadership
Clinical pathology knowledge
Communication skills
Teamwork

Education

Bachelor of Science in Medical/Clinical Laboratory Sciences
Veterinary Technician certification (preferred)
ASCP Certification (preferred)

Tools

Laboratory equipment
Laboratory information management systems
Job description
Overview

Company: Toxicologic Pathology Associates (TPA), Inc.

Location: Jefferson, Arkansas, United States

Job Title: Clinical Pathology Services Manager (Onsite)
(Medical Technologist/Medical Laboratory Scientist/Veterinary Technician - Specialist in Clinical Pathology)

Position Description

Toxicologic Pathology Associates, Inc (TPA) is looking for an experienced Clinical Pathology Manager to join our team at the Food and Drug Administration’s National Center for Toxicological Research (NCTR) in Jefferson (Little Rock Metro area), Arkansas. TPA’s clinical pathology laboratory routinely performs hematology, clinical chemistry, urinalysis, hormone assays (ELISA) and other specialty testing on diagnostic/research samples collected from a variety of species, including rats, mice, guinea pigs, minipigs and non-human primates. TPA is an onsite contractor of the FDA and provides pathology and pathology-related services to the NCTR research community. The successful candidate will routinely collaborate with NCTR investigators. Regular workdays are Monday to Friday, with regular work hours from 7am to 5pm. Weekend duty expectations are occasional and on an as-needed basis.

Education
  • Bachelor of Science degree in Medical/Clinical Laboratory Sciences, Medical Technology, or other related field from an accredited institution.
  • Graduate of American Veterinary Medical Association accredited Veterinary Technician program.
  • Successful completion of an official military training of at least 50 weeks duration, and who have held the military enlisted occupational specialty of Medical Laboratory Specialist (Laboratory Technician).
  • The American Society for Clinical Pathology (ASCP) or equivalent Generalist Clinical Laboratory Scientist Certification (CLS) or Academy of Veterinary Clinical Pathology Technician (AVCPT) Certification preferred.
Experience
  • Minimum two-year of intensive experience of working in a clinical pathology laboratory.
  • Medical or Veterinary Technologist experience in a supervisory capacity or in a senior role or experience of working in a research laboratory is preferred.
Expectations
  • General knowledge of laboratory methodologies, laboratory equipment, interpretation of results, and quality control.
  • Demonstrated hands-on ability to perform all tasks in a standard clinical pathology laboratory with high degree of accuracy.
  • Experience of writing standard laboratory operating procedures and is willing to develop, validate and write new procedures, when required.
  • Must perform effectively as a team member, maintain a positive atmosphere, supervise laboratory staff, communicate professionally and effectively with management, coworkers, and customers.
  • Assist investigators in determining specific tests/test requirements for individual studies and determine cost/labor needed to complete studies.
  • Perform routine/specialized procedures on blood, urine, tissues, and other body fluids of a variety of animal species in accordance with established protocols/SOPs and provide results.
  • Ensure compliance with standard operating procedures (SOPs) and that all work is performed in compliance with FDA/EPA Good Laboratory Practice regulations.
  • Maintain safety through appropriate use of personal protective equipment and by observing safe work practices.
  • Collect blood from laboratory animals at necropsy and prepare for storage or analysis.
  • Excellent written and oral communication skills are essential.
  • Maintenance and review of a quality control program.
  • Perform equipment maintenance as required.
  • Order supplies and any other assigned tasks.
How to Apply / Contact

TPA provides a comprehensive benefits package to its employees and a competitive starting salary commensurate with experience, expertise and skill set. Employment of successful candidates will be contingent upon receipt of a satisfactory drug screening report, obtaining the necessary federal government security clearance and successful passing of a required physical examination. Drug screening is provided by an off-site third party and is paid for by TPA. The annual physical examination is provided by the NCTR Occupational Medical Program and is at no cost to the employee. The candidate should be eligible to work in the United States.

TPA is an equal opportunity employer. We do not unlawfully discriminate against any applicant because of race, sex, gender, ethnicity, religion, creed, age, color, military/veteran status, genetic condition or information, sexual orientation, gender identity, national origin, ancestry, marital status, qualified physical or mental disability, transgender status, or any other legally protected class in accordance with federal, state and local laws.

Interested candidates should submit their resume and contact information to Kimberly.maynard@fda.hhs.gov. The application review will start immediately, and the position will remain open until filled.

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