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The People Behind OncoSure

Combining medical, scientific, and operational expertise to advance cancer diagnostics and personalized genetic testing — for earlier answers and better outcomes.
Double Board-Certified
Cecilia Oliveri, MD
Laboratory Director
Anatomic and Clinical Pathologist Cytopathologist
Education:
Universidad Central de Venezuela, Caracas
University of South Florida (Fellowship)
University of South Alabama (Fellowship)
Areas of Expertise:
Anatomic & Clinical Pathology
Oncologic Surgical Pathology
Gastrointestinal Pathology
Cytopathology
Laboratory Operations
Dr Cecilia Oliveri is a highly accomplished and respected physician double boarded in Anatomic and Clinical
Pathology, Cytopathology, Oncologic Surgical Pathology and Gastrointestinal Pathology.

She earned her Doctor of Medicine degree from Universidad Central de Venezuela, Caracas, Venezuela. Dr
Cecilia Oliveri completed a prestigious fellowship in Oncologic Surgical Pathology and Cytopathology at the
renowned H Lee Moffitt Cancer Center and Research Institute, University of South Florida and Anatomic and
Clinical Pathology at the University of South Alabama College of Medicine Mobile, Alabama.

As a double board-certified physician in Anatomic and Clinical Pathologist and Cytopathologist and Oncologic
Surgical Pathology, Dr. Oliveri has authored numerous peer- reviewed publications and brings a wealth of
clinical knowledge and expertise to her capacity as Clinical Laboratory Director.

Dr. Cecilia Oliveri will exercise overarching leadership of the laboratory’s clinical operations and ensure
rigorous adherence to CLIA and all pertinent federal, state and accrediting‑body standards are upheld to the
highest levels of diagnostic accuracy and quality control. In this capacity, she will direct and supervise
laboratory personnel, lead the development of advanced testing methodologies and implement a
comprehensive quality‑management framework to govern test validation, monitoring accuracy and
performance metrics, to ensure the delivery of reliable and clinically actionable patient results.

As Clinical Laboratory Director, Dr. Cecilia Oliveri will also conduct formal competency assessments to
optimize professional development, workforce performance and operational efficiency. Additionally, she will
offer expert consultation and support to our healthcare community, contributing to high‑quality patient care
and informed clinical decision‑making.
CLIA Supervisor
Stephanie Altidort
General Supervisor, Molecular Pathology
Molecular Diagnostics & Genomics
Education:
Florida Atlantic University (BS Neuroscience)
Areas of Expertise:
High-Complexity Testing
Quality Control
Staff Management
Stephanie Altidort is a laboratory professional with a strong academic foundation and technical expertise in molecular diagnostics and genomic science. She earned her Bachelor of Science in Neuroscience from Florida Atlantic University, where she developed a foundational understanding of neurobiological processes and cellular mechanisms relevant to molecular medicine. She holds certification as a Molecular Diagnostics Technologist through the American Medical Technologists and is currently pursuing board certification in Cytogenetics through the American Society for Clinical Pathology. Ms. Altidort is licensed as a Florida Supervisor in Molecular Pathology by the Florida Department of Health and maintains certification in Basic Life Support through the National CPR Foundation.

In her role as General Supervisor, Ms. Altidort is entrusted with critical responsibilities aligned with Clinical Laboratory Improvement Amendments (CLIA) regulatory standards. She provides direct supervision of high-complexity molecular testing procedures, ensuring the integrity and validity of all phases of laboratory operations. Her responsibilities include reviewing and authorizing test procedures, monitoring quality assurance and quality control systems, and validating instrument performance to uphold analytical accuracy and reproducibility.

Ms. Altidort plays an integral role in personnel management, including the evaluation of staff competency, coordination of continuing education, and oversight of protocol adherence. She collaborates with the laboratory director and technical leadership in the implementation of new assays, assessment of workflow efficiency, and maintenance of documentation required for regulatory compliance and laboratory accreditation.

With a commitment to scientific rigor and operational excellence, Ms. Altidort advances the quality of diagnostic services through precise supervision, regulatory expertise, and a focus on clinical impact. Her contributions are essential to maintaining the laboratory’s adherence to best practices and its mission of delivering accurate, timely, and clinically actionable results.

20+ Years Experience
William Wysock
Molecular Scientist
Validation & Process Development
Education:
Catholic University of America (MS Biology)
Loyola University (BA Writing)
Areas of Expertise:
Method Validation
NGS Technologies
Six Sigma Quality
William Wysock is a seasoned molecular scientist with over two decades of experience in clinical and translational research, specializing in molecular diagnostics and infectious disease biology. He holds a Bachelor of Arts in Writing from Loyola University of Maryland and a Master of Science in Biology from the Catholic University of America. His unique interdisciplinary background combines scientific rigor with clear, analytical communication, a valuable asset in both research and laboratory operations.

Mr. Wysock is certified in Molecular Biology by the American Society for Clinical Pathology and has extensive expertise in advanced molecular methodologies, including polymerase chain reaction (PCR) techniques, next-generation sequencing (NGS), and the implementation of laboratory quality systems. He is also trained in Six Sigma methodologies and holds a Green Belt certification, underscoring his commitment to operational efficiency and process improvement.

In his role as Molecular Scientist, Mr. Wysock is principally responsible for overseeing the laboratory's validation processes. This includes designing and executing method verification studies, analyzing performance metrics, and ensuring all assays meet stringent analytical and clinical standards prior to implementation. His in-depth knowledge of assay development and regulatory requirements plays a critical role in maintaining the scientific credibility and compliance integrity of the laboratory.

Mr. Wysock also serves as the laboratory’s primary resource for complex technical inquiries. He provides expert guidance on molecular workflows, troubleshooting protocols, and optimizing assay performance, thereby supporting both day-to-day operations and long-term innovation. His leadership in this capacity ensures that laboratory personnel are equipped with the technical insights necessary for high-complexity testing.

A prolific contributor to the scientific literature, Mr. Wysock has authored numerous peer-reviewed publications in the fields of molecular diagnostics and infectious disease research. His scholarly work reflects a sustained commitment to advancing laboratory science and integrating evidence-based practices into clinical diagnostics. Through his analytical acumen, mentorship, and research-driven approach, William Wysock significantly enhances the laboratory's capacity for precision medicine and scientific advancement.

Why Choose OncoSure Testing?

24 Hours

Rapid results when it matters most

97.77%

Confidence you can rely on

Non-Invasive

Just one blood draw needed

207+ Cancers

For complete peace of mind
Clinical Support: (888) 925-4816
All Major Insurance Accepted
CLIA-certified laboratory
OncoSure
CANCER & GENETIC TESTING
Leading provider of comprehensive cancer screening services, supporting early detection and empowering every healthcare journey.
Clinical Support
1-888-925-4816
Address
1100 Park Central Blvd S suite 1700

Pompano Beach, Florida 33064
This test was developed, and its performance characteristics were determined by OncoSure Laboratories. It has not been cleared or approved by the U.S. Food and Drug Administration. The test was performed in a CLIA-certified laboratory and is intended for clinical purposes. OncoSure Laboratories is also COLA-accredited, having received a perfect score on its most recent inspection.
CLIA Accredited Laboratory
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Medicare/ Medicaid & PPO Plans Accepted
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