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Posted Apr 27, 2026

Clinical Laboratory Operations Programming Lead - FSP

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PXL is seeking an operations lead with expertise in lab operations and proficiency in computational programming to support the generation and delivery of quality biomarker samples and data. Job Responsibilities: • Establish and streamline SKDL processes to increase efficiency and implement analytical tools to advance departmental goals. • Support SKDL operations, including samples, kits, and data processes, ensuring integrity and completeness for database locks. • Use technical tools/systems and programming languages to systematically clean data, including processing confidential data according to guidelines. • Programmatically aggregate and extract key information from operational reports • Possess knowledge of structured data, such as entities, classes, hierarchies, relationships, and metadata, with the ability to perform data mapping • Support processing of informed consent forms (ICFs) and ensure compliance with ICFs for internal sample handling, tracking, usage, and destruction. • Maintain and review metrics related to clinical study samples, data, kits, and logistics. • Lead cross-functional study teams, manage vendor relationships, and oversee clinical trial biosamples and data monitoring. • Support clinical trial biosamples and data monitoring and completeness from collection through to disposal, per requirements of the study • Anticipate challenges, manage dependencies, and mitigate risks across SKDL projects. • Enhance communication with senior stakeholders and align SKDL functions with group objectives. • Participate in vendor oversight activities, including issue escalation, metrics reviews, and performance monitoring Job Requirements: • Proficiency in one or more programming languages (R, Python, Perl, SQL, MATLAB) • Familiarity with APIs, database development, dashboard development, and Linux/Unix environments • Ability to critically analyze and plan for sample interdependencies, risks, and issues with an awareness of the impacts to clinical studies/program. • Strong problem-solving, project management, and organizational skills, with ability to effectively multi-task and prioritize. • Extensive process development and project management experience including vendor management • Excellent oral and written communication and presentation skills • Advanced excel knowledge required • 6-7 years of experience in lab operations and programming preferred. Education: • Bachelor’s or master’s degree. Experience: • 6+ years of clinical research experience in academic, CRO, or pharmaceutical/biotech settings, with knowledge of clinical trials and clinical databases. #LI-LO1 #LI-REMOTE