Jessica Parkman brings extensive experience across the biotechnology landscape, with a background spanning genomics, diagnostics, medical devices, and pharmaceutical organizations. She works at the intersection of science, technology, and regulated environments, leading complex initiatives in product strategy, system implementation, and operational transformation -- and is known for bringing structure and clarity to highly ambiguous challenges.
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"What I enjoy most is working through complex challenges and helping teams turn them into something clear and actionable."
Jessica has designed and implemented scalable frameworks, led process improvement efforts, and aligned cross-functional teams to drive meaningful, sustainable outcomes. Her work connects business strategy with technical execution, ensuring organizations can operate efficiently while meeting regulatory and quality standards across FDA compliance, lab operations, and patient privacy. She has guided organizations through large-scale workflow and operational transformations, helping teams move from concept to execution in environments where precision, compliance, and scalability are non-negotiable.
Outside of work, Jessica enjoys fishing and tabletop games with her family.
Partner with our clinical regulation leaders to draft a comprehensive plan of action that drives your existing CLIA, CAP, and NYS LIS and LIMS systems, policies, and SOPs toward FDA LDT Final Rule compliance.
Harness decades of our clinical regulatory experience to develop compliant lab procedures addressing logistics and reporting needs while optimizing your day-to-day operations, resources, and data processing operations.
Protect sensitive patient information and maintain data privacy and security standards in alignment with HIPAA and additional local regulations.
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