MOLECULAR PATHOLOGY TECH

Moffitt Cancer Center; United States; On-site; USD 50,000 - 76,000; Full time

Job summary

Moffitt Cancer Center in Florida is seeking a Molecular Pathology Technologist to join a collaborative clinical laboratory team. The role focuses on DNA/RNA isolation, PCR techniques, sequencing, assay validation, quality control and timely reporting of results.

The ideal candidate holds a Master’s degree in Molecular Biology, ASCP certification and a strong ability to work independently, maintain equipment, and train other staff while upholding strict QA/QC standards.

Qualifications

• Master’s degree in Molecular Biology or related field preferred.
• ASCP certification preferred.
• 12 months experience in molecular pathology, medical technology or related field.

Responsibilities

• Specimen handling and accessioning for clinical analysis.
• Accurately verifies orders and enters specimen collection information.
• Perform molecular pathology testing according to SOPs and QC/QA requirements.
• Maintain equipment and records; perform preventive maintenance.

Skills

ASCP certified

Education

Bachelor’s Degree in Molecular Biology, Medical technology or Biologic Science

Licensed Medical Technologist with Molecular Specialty (Florida)

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.

As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.

Summary

Possesses a working knowledge of molecular and cell biology with experience in the performance and application of techniques used in clinical molecular diagnostic testing including DNA and RNA isolation, conventional and real-time PCR, quantitative and qualitative reverse transcriptase PCR (RT-PCR), automated DNA sequencing and fragment analysis, restriction enzyme digestion, gel electrophoresis, other molecular diagnostic techniques and general assay validation and quality control/quality assurance. Experience with in house molecular diagnostic assay design and development, including design of primers and probes, and assay validation, quality control, quality assurance, and/or troubleshooting, is desirable. The ability to follow the standard protocol and independently perform laboratory routine testing in the area of molecular pathology is required.

In addition to the above, the individual will be expected to maintain equipment and records; perform quality control and quality assurance activities, participate in the evaluation of new procedures and equipment; provide training for technologists, residents, fellows, and other medical staff; work efficiently in a computerized environment; assist with the functions required to maintain the smooth operation of the department such as clerical duties, reagent preparation, and inventory control; and write and revise technical procedures.

The molecular pathology technologist requires minimal oversight to complete assigned tasks. Possesses superior organizational skills and is capable of working independently.

This position will work under the scientific direction of the Medical Director and Coordinator of Molecular Pathology.

Position Highlights:

• Specimen handling: Receives, accessions, and processes blood, and a variety of other human source specimens, for clinical analysis.
• Molecular Pathology Testing: Performs and reports tests according to standard operating procedures as established in the clinical molecular laboratory. Demonstrates a thorough knowledge of molecular testing theory and scientific principles, routine testing procedures, and instrument operation and maintenance requirements, as they apply to molecular testing.

The Ideal Candidate:

• Master’s degree in Molecular Biology.
• ASCP certified.
• Possesses superior organizational skills, and is capable of working independently.

Responsibilities:

• Specimen handling: Receives, accessions, and processes blood, and a variety of other human source specimens, for clinical analysis.
• Accurately verifies orders and enters specimen collection information into the laboratory computer system.
• Consistently complies with specimen rejection criteria. Accepts only suitable specimens for analysis. Follows established policies for notification and documentation of unacceptable specimens. Accurately labels all specimens received in accordance with established policies.
• Demonstrates a thorough working knowledge of the laboratory computer system order entry and specimen accessioning functions, including a sound working knowledge of data entry and specimen requirements.
• Demonstrates the analytical ability to troubleshoot and resolve problems related to specimen collection and processing.
• Molecular Pathology Testing: Performs and reports tests according to standard operating procedures as established in the clinical molecular laboratory. Demonstrates a thorough knowledge of molecular testing theory and scientific principles, routine testing procedures, and instrument operation and maintenance requirements, as they apply to molecular testing.
• Consistently follows departmental procedures for test performance in order to ensure accurate testing results.
• Consistently reports results within established turn around times. Is able to prioritize and organize workflow in order to meet turn around time requirements.
• Thoroughly reviews all work prior to release of patient data, in order to prevent clerical errors and amended reports, generating no more than 2 amended reports due to clerical errors annually.
• Always follows established policies and procedures related to quality control requirements and acceptability of data. Never reports patient results if QC is not within acceptable limits.
• Performs and documents preventive maintenance as scheduled in a thorough, careful manner.
• Demonstrates the ability to independently troubleshoot and resolve problems associated with abnormal specimens and discrepant test results.
• Demonstrates the ability to independently troubleshoot and resolve a wide variety of procedural, instrument, and specimen problems.

Credentials and Qualifications:

• Bachelor’s Degree in Molecular Biology, Medical technology or Biologic Science is required.
• Licensed Medical Technologist with Molecular Specialty by the state of Florida required.
• Must possess 12 months experience in molecular pathology, medical technology or related field to include experience related to nucleic acid extraction and amplification by PCR techniques, DNA sequencing, mutation analysis, molecular oncology, appropriate specimen handling, quality control, and quality assurance as related to molecular laboratory techniques.
• Sound technical knowledge of specialty as it relates to test validation, performance, QC, and QA activities knowledge of all applicable laboratory regulations required.”

Salary Range

$36.13 - $55.15

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Moffitt Career Site

1. Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

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