Clinical Development Project Manager

🕒 November 6

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

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• Open for 9 days.
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• No salary listed.

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Baylor Genetics

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1978

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Healthcare • Consulting • Food & Beverage

Baylor Genetics is a clinical genomics and precision diagnostics laboratory affiliated with Baylor College of Medicine that provides comprehensive genetic testing and interpretation services. The company offers whole genome and whole exome sequencing, chromosomal microarray analysis, mitochondrial testing, pharmacogenomics, and specialized assays, along with genetic counseling, provider support, and insurance/payment resources. Baylor Genetics supports healthcare providers, researchers, and families with AI-enhanced interpretation, multimodal data integration, and end-to-end clinical and laboratory services.

📋 Description

• Lead execution of Clinical Development projects, ensuring milestones are achieved on time, within scope, and in alignment with clinical and organizational priorities • Develop and manage detailed project plans, dependency maps, and risk registers • Proactively mitigate delivery, data, and validation risks across dry lab workflows • Coordinate cross-functional teams across bioinformatics, software engineering, clinical operations, and product • Drive execution, resolve blockers, and ensure accountability for deliverables • Translate complex analytical and computational requirements into clear, executable project deliverables • Support scalable and compliant genomic analysis and reporting • Monitor and analyze project performance metrics, including timeline adherence, risk trends, and validation readiness • Report project status, risks, and outcomes to program leadership through clear, data-driven updates and summaries • Support documentation, audits, and validation activities to ensure regulatory, quality, and data-governance compliance • Perform other duties as assigned to support team and organizational objectives • Comply with company policies, procedures, and applicable regulatory requirements

🎯 Requirements

• Bachelor’s degree in Life Sciences, Genetics, Molecular Biology, Public Health, Healthcare Administration, Clinical Research, or related field • Minimum 4 years of relevant experience in clinical lab operation, development and research, diagnostics, biotechnology, healthcare, or related fields • At least 2 years managing cross-functional projects with accountability for timelines and deliverables • Demonstrated ability to manage multiple technically complex projects simultaneously • Extensive experience managing cross-functional teams, including bioinformatics scientists, software engineers, analysts, and clinical stakeholders • Proven experience working with data pipelines, analytical workflows, or laboratory informatics platforms • Strong understanding of technical dependencies, system integrations, and validation considerations in regulated environments • Excellent communication, organizational, and leadership skills • Effective interpersonal, negotiation, and technical meeting facilitation skills • Demonstrated ability to lead teams through ambiguity, evolving technical requirements, and data-driven decision-making • Ability to collaborate effectively with stakeholders at all levels, including highly technical and non-technical audiences • Strong analytical and problem-solving skills, with the ability to identify and mitigate technical and delivery risks • Strong attention to detail, data accuracy, and process rigor • Passion for continuous improvement and operational excellence • Equivalent combination of education and experience may be considered • Master’s degree in life science, or a related field (preferred) • Project management certifications (PMP or equivalent) (preferred)

🏖️ Benefits

• May require occasional travel to conferences, partner sites, healthcare institutions, or company meetings

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